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Johnson & Johnson
FDA Orange Book

Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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Jai Radhe Sales is your partner for all your sourcing needs.

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Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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Johnson & Johnson

VISIT THE VIRTUAL BOOTH, Contact Details

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Review portfolio & marketing content
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EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

DIGITAL CONTENT

INTERVIEW #SpeakPharma, VLOG #PharmaReel, DATA COMPILATION #PharmaFlow, 4373 NEWS #PharmaBuzz

INTERVIEW #SpeakPharma
VLOG #PharmaReel
DATA COMPILATION #PharmaFlow
4373 NEWS #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

118 All APIs, 88 USDMF, 47 CEP/COS, 11 JDMF, 26 KDMF, 30 NDC API, 1 VMF

118 All APIs
88 USDMF
47 CEP/COS
11 JDMF
26 KDMF
30 NDC API
1 VMF

DEVELOPMENTS

502 Drugs in Development

502 Drugs in Development

FINISHED DOSAGE FORMULATIONS

1589 FDF Dossiers, 354 FDA Orange Book, 90 Europe, 508 Canada, 245 Australia, 390 South Africa, 2 Listed Dossiers

1589 FDF Dossiers
354 FDA Orange Book
90 Europe
508 Canada
245 Australia
390 South Africa
2 Listed Dossiers

EXCIPIENTS

1 All Excipients, 1 USDMF

1 All Excipients
1 USDMF

INSPECTIONS & REGISTRATIONS

36 FDA, 27 EDQM, 2 WHO-GMP, 5 GDUFA

36 FDA
27 EDQM
2 WHO-GMP
5 GDUFA

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FILTER :

filter Active Ingredients Reset all filters

354 All

01 1ABCIXIMAB

02 2ABIRATERONE ACETATE

03 2ABIRATERONE ACETATE; NIRAPARIB TOSYLATE

04 5ACETAMINOPHEN

05 11ACETAMINOPHEN; CODEINE PHOSPHATE

06 1ACETAMINOPHEN; HYDROCODONE BITARTRATE

07 2ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

08 1ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE; OXYCODONE TEREPHTHALATE

09 1ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE

10 1ACETRIZOATE SODIUM

11 1ACETYLCYSTEINE; ISOPROTERENOL HYDROCHLORIDE

12 2ALMOTRIPTAN MALATE

13 1AMIVANTAMAB-VMJW

14 2APALUTAMIDE

15 1ASPIRIN; METHOCARBAMOL

16 2BEDAQUILINE FUMARATE

17 3BEPRIDIL HYDROCHLORIDE

18 3BUDESONIDE

19 1CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE

20 2CANAGLIFLOZIN

21 8CANAGLIFLOZIN; METFORMIN HYDROCHLORIDE

22 2CARBINOXAMINE MALEATE

23 13CETIRIZINE HYDROCHLORIDE

24 1CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

25 3CHLORHEXIDINE GLUCONATE

26 2CHLORZOXAZONE

27 4CISAPRIDE MONOHYDRATE

28 1CLADRIBINE

29 1COBICISTAT; DARUNAVIR

30 1COBICISTAT; DARUNAVIR; EMTRICITABINE; TENOFOVIR ALAFENAMIDE FUMARATE

31 2CYCLOBENZAPRINE HYDROCHLORIDE

32 2DARATUMUMAB

33 1DARATUMUMAB AND HYALURONIDASE-FIHJ

34 7DARUNAVIR

35 2DESOGESTREL; ETHINYL ESTRADIOL

36 1DIENESTROL

37 6DIPHENHYDRAMINE HYDROCHLORIDE

38 3ERDAFITINIB

39 1ERYTHROMYCIN

40 1ESKETAMINE HYDROCHLORIDE

41 3ESTRADIOL

42 1ETHINYL ESTRADIOL; NORELGESTROMIN

43 12ETHINYL ESTRADIOL; NORETHINDRONE

44 7ETHINYL ESTRADIOL; NORGESTIMATE

45 3ETRAVIRINE

46 5FAMOTIDINE

47 6FENTANYL

48 1FLAVOXATE HYDROCHLORIDE

49 7GALANTAMINE HYDROBROMIDE

50 2GOLIMUMAB

51 4GRISEOFULVIN, MICROCRYSTALLINE

52 1GUSELKUMAB

53 7HALOPERIDOL

54 2HALOPERIDOL DECANOATE

55 2HALOPERIDOL LACTATE

56 23IBUPROFEN

57 2IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

58 1IMCIROMAB PENTETATE

59 1INFLIXIMAB

60 4ITRACONAZOLE

61 4KETOCONAZOLE

62 1KETOTIFEN FUMARATE

63 2LAZERTINIB MESYLATE

64 1LEUPROLIDE ACETATE

65 1LEVAMISOLE HYDROCHLORIDE

66 9LEVOFLOXACIN

67 7LOPERAMIDE HYDROCHLORIDE

68 2LOPERAMIDE HYDROCHLORIDE; SIMETHICONE

69 2MEBENDAZOLE

70 1MECLOCYCLINE SULFOSALICYLATE

71 6MESTRANOL; NORETHINDRONE

72 4METHYLPHENIDATE HYDROCHLORIDE

73 2METRONIDAZOLE

74 1MICONAZOLE

75 2MICONAZOLE NITRATE

76 5MINOXIDIL

77 1NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE

78 1NESIRITIDE

79 1NICOTINE

80 1NONOXYNOL-9

81 1NORETHINDRONE

82 8OFLOXACIN

83 5OXYBUTYNIN CHLORIDE

84 1OXYMETAZOLINE HYDROCHLORIDE

85 9PALIPERIDONE

86 11PALIPERIDONE PALMITATE

87 1PENTOSAN POLYSULFATE SODIUM

88 2PSEUDOEPHEDRINE HYDROCHLORIDE

89 2RILPIVIRINE HYDROCHLORIDE

90 17RISPERIDONE

91 9RIVAROXABAN

92 1SIMEPREVIR SODIUM

93 2TALQUETAMAB-TGVS

94 2TECLISTAMAB-CQYV

95 3TERCONAZOLE

96 5THEOPHYLLINE

97 3TOLMETIN SODIUM

98 9TOPIRAMATE

99 1TRABECTEDIN

100 2TRAMADOL HYDROCHLORIDE

101 2TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)

102 3USTEKINUMAB

filter Dosage Reset all filters

354 All

01 2AEROSOL, FOAM;TOPICAL

02 1AEROSOL;VAGINAL

03 5CAPSULE, EXTENDED RELEASE;ORAL

04 1CAPSULE; ORAL

05 16CAPSULE;ORAL

06 1CONCENTRATE;ORAL

07 1CREAM, SUPPOSITORY;TOPICAL, VAGINAL

08 2CREAM;TOPICAL

09 4CREAM;VAGINAL

10 1DRUG-ELUTING CONTACT LENS;OPHTHALMIC

11 3ELIXIR;ORAL

12 8FILM, EXTENDED RELEASE;TRANSDERMAL

13 1FOR SOLUTION;INTRAVENOUS

14 1FOR SUSPENSION;ORAL

15 1IMPLANT;IMPLANTATION

16 5INJECTABLE; INJECTION

17 30INJECTABLE;INJECTION

18 4INJECTABLE;INTRAMUSCULAR

19 1POWDER;INTRAVENOUS

20 1SHAMPOO;TOPICAL

21 2SOLUTION/DROPS;OPHTHALMIC

22 1SOLUTION;INHALATION

23 1SOLUTION;INTRAUTERINE

24 10SOLUTION;ORAL

25 5SOLUTION;TOPICAL

26 1SPONGE;TOPICAL

27 3SPRAY, METERED;NASAL

28 1SPRAY;NASAL

29 2SUPPOSITORY;RECTAL

30 1SUPPOSITORY;VAGINAL

31 11SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR

32 2SUSPENSION/DROPS;ORAL

33 8SUSPENSION;ORAL

34 1SWAB;TOPICAL

35 1SYRUP;ORAL

36 3SYSTEM;TRANSDERMAL

37 17TABLET, CHEWABLE;ORAL

38 4TABLET, EXTENDED RELEASE; ORAL

39 21TABLET, EXTENDED RELEASE;ORAL

40 1TABLET, FOR SUSPENSION;ORAL

41 7TABLET, ORALLY DISINTEGRATING;ORAL

42 1TABLET; ORAL-21

43 1TABLET; ORAL-28

44 130TABLET;ORAL

45 13TABLET;ORAL-21

46 13TABLET;ORAL-28

47 1TABLET;VAGINAL

48 1TAMPON;VAGINAL

49 2VIAL

filter Dosage Strength Reset all filters

354 All

01 10.01%

02 10.025%

03 10.025%;0.3%

04 10.025MG,0.025MG,0.025MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

05 10.032MG/INH

06 10.032MG/SPRAY

07 20.035MG,0.035MG,0.035MG; 0.18MG,0.215MG,0.25MG

08 20.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

09 10.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG

10 10.035MG,0.035MG,0.035MG;0.5MG,0.75MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

11 10.035MG,0.035MG;0.5MG,1MG

12 30.035MG,0.035MG;0.5MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

13 10.035MG/24HR;0.15MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

14 20.035MG;0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

15 10.035MG;0.5MG

16 10.035MG;0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

17 20.035MG;1MG

18 20.035MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

19 10.05MG/24HR

20 20.05MG;1MG

21 10.064MG/INH

22 10.06MG;10MG

23 10.075MG/24HR

24 20.08MG;1MG

25 20.15MG;0.03MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

26 10.1MG/24HR

27 10.1MG;2MG

28 10.25MG

29 10.35MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

30 10.4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

31 10.5%

32 10.5MG

33 20.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

34 10.8% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

35 11%

36 11.092GM/3.5ML (312MG/ML)

37 11.2GM;2%

38 11.560GM/5ML (312MG/ML)

39 11.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

40 11.5MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

41 110%;0.05%

42 1100MCG/HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

43 14100MG

44 2100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

45 3100MG/5ML

46 1100MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

47 1100MG/5ML;15MG/5ML

48 3100MG/ML

49 810MG

50 510MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

51 410MG/ML

52 1112.5MG/15ML

53 1117MG/0.75ML (117MG/0.75ML)

54 112.5%

55 112.5MCG/HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

56 112.5MG/5ML

57 112.5MG/VIAL

58 2120MG

59 1120MG/5ML;12MG/5ML

60 1120MG;2000UNITS/ML

61 2125MG

62 1125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

63 112MG

64 112MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

65 1130MG/26ML

66 1150MG

67 2150MG;1GM

68 2150MG;500MG

69 1150MG;800MG

70 1150MG;800MG;200MG;EQ 10MG BASE

71 1153MG/1.7ML(90MG/ML)

72 1156MG/ML (156MG/ML)

73 315MG

74 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

75 115MG/16HR

76 1184MG;143.75MG;172.5MG

77 118MG

78 21MG

79 21MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

80 21MG/5ML

81 11MG/7.5ML

82 21MG/ML

83 11MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

84 11MG/VIAL

85 22%

86 32% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

87 32.5MG

88 10200MG

89 2200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

90 1200MG;30MG

91 420MG

92 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

93 120MG/ML

94 1225MG

95 1234MG/1.5ML (156MG/ML)

96 2240MG

97 4250MG

98 2250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

99 1250MG/10ML

100 125MCG/HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

101 425MG

102 125MG/VIAL

103 1273MG/0.875ML (273MG/0.875ML)

104 127MG

105 32MG

106 42MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

107 12MG/ML

108 22MG;125MG

109 13.7%;2.86%;3.42%

110 3300MG

111 3300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

112 1300MG;15MG

113 2300MG;30MG

114 2300MG;60MG

115 1300MG;7.5MG

116 130MG/3ML(10MG/ML)

117 1325MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

118 1325MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

119 1325MG;37.5MG

120 1325MG;400MG

121 1325MG;5MG

122 1325MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

123 1325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

124 1350MG/7ML(50MG/ML)

125 136MG

126 137.5MCG/HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

127 137.5MG/VIAL

128 139MG/0.25ML (39MG/0.25ML)

129 43MG

130 13MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

131 13MG/1.5ML(2MG/ML)

132 24%

133 3400MG

134 3400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

135 2400MG/100ML

136 1400MG/20ML

137 440MG/ML

138 1410MG/1.315ML (311.79MG/ML)

139 145MG/0.5ML

140 24MG

141 24MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

142 14MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

143 14MG/ML

144 14MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

145 35%

146 4500MG

147 2500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

148 1500MG;4.5MG;0.38MG

149 2500MG;5MG

150 1500MG;EQ 100MG BASE

151 1500MG;EQ 50MG BASE

152 150MCG/HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

153 550MG

154 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

155 150MG/4ML

156 250MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

157 150MG/VIAL

158 250MG;1GM

159 250MG;500MG

160 153%

161 1546MG/1.75ML (312MG/ML)

162 154MG

163 45MG

164 65MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

165 25MG/5ML

166 25MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

167 15MG;120MG

168 2600MG

169 1600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

170 160MG

171 3650MG

172 26MG

173 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

174 175MCG/HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

175 175MG

176 178MG/0.5ML (78MG/0.5ML)

177 1800MG

178 1800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

179 1800MG;10MG;165MG

180 180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

181 1819MG/2.625ML (312MG/ML)

182 190MG/1ML

183 29MG

184 1EQ 100MG BASE

185 1EQ 100MG BASE/ML

186 1EQ 10MG BASE

187 1EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

188 1EQ 12MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

189 1EQ 150MG BASE

190 1EQ 16MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

191 1EQ 19MCG BASE

192 1EQ 1MG BASE/ML

193 1EQ 2.5MG BASE

194 1EQ 200MG BASE

195 3EQ 20MG BASE

196 1EQ 240MG BASE

197 1EQ 24MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

198 1EQ 250MG/50ML (EQ 5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

199 1EQ 25MG BASE

200 1EQ 28MG BASE

201 1EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

202 1EQ 400MG BASE

203 1EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

204 1EQ 500MG/100ML (EQ 5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

205 1EQ 500MG/20ML (EQ 25MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

206 1EQ 50MG BASE

207 1EQ 50MG BASE/ML

208 1EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

209 1EQ 6.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

210 1EQ 600MG BASE

211 1EQ 65MG BASE

212 1EQ 750MG/150ML (EQ 5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

213 1EQ 750MG/30ML (EQ 25MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

214 1EQ 80MG BASE

215 2EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

216 1N/A

filter Regulatory Info Reset all filters

354 All

01 208DISCN

02 34OTC

03 81RX

04 31Blank

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Supplier Virtual Booth

price-trend

01

Brand Name : REOPRO

Fi Europe 2024

Not Confirmed

Brand Name : REOPRO

Fi Europe 2024

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RLD :

TE Code :

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : REOPRO

Dosage Strength : 2MG/ML

Approval Date :

Application Number : 103575

RX/OTC/DISCN :

RLD :

TE Code :

Product
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02

Brand Name : ZYTIGA

Fi Europe 2024

Not Confirmed

Brand Name : ZYTIGA

Fi Europe 2024

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RLD : Yes

TE Code : AB

ABIRATERONE ACETATE

Dosage Form : TABLET; ORAL

Proprietary Name : ZYTIGA

Dosage Strength : 250MG

Approval Date : 2011-04-28

Application Number : 202379

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Product
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03

Brand Name : ZYTIGA

Fi Europe 2024

Not Confirmed

Brand Name : ZYTIGA

Fi Europe 2024

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RLD : Yes

TE Code : AB

ABIRATERONE ACETATE

Dosage Form : TABLET; ORAL

Proprietary Name : ZYTIGA

Dosage Strength : 500MG

Approval Date : 2017-04-14

Application Number : 202379

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

Product
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04

Brand Name : AKEEGA

Fi Europe 2024

Not Confirmed

Brand Name : AKEEGA

Fi Europe 2024

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RLD : Yes

TE Code :

ABIRATERONE ACETATE; NIRAPARIB TOSYLATE

Dosage Form : TABLET; ORAL

Proprietary Name : AKEEGA

Dosage Strength : 500MG;EQ 50MG BASE

Approval Date : 2023-08-11

Application Number : 216793

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Product
Web Link

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05

Brand Name : AKEEGA

Fi Europe 2024

Not Confirmed

Brand Name : AKEEGA

Fi Europe 2024

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RLD : Yes

TE Code :

ABIRATERONE ACETATE; NIRAPARIB TOSYLATE

Dosage Form : TABLET; ORAL

Proprietary Name : AKEEGA

Dosage Strength : 500MG;EQ 100MG BASE

Approval Date : 2023-08-11

Application Number : 216793

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Product
Web Link

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06

Brand Name : TYLENOL

Fi Europe 2024

Not Confirmed

Brand Name : TYLENOL

Fi Europe 2024

Not Confirmed

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RLD : No

TE Code :

ACETAMINOPHEN

Johnson & Johnson

Dosage Form : SUPPOSITORY; RECTAL

Proprietary Name : TYLENOL

Dosage Strength : 650MG

Approval Date : 1982-01-01

Application Number : 17756

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
Web Link

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07

Brand Name : TYLENOL

Fi Europe 2024

Not Confirmed

Brand Name : TYLENOL

Fi Europe 2024

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RLD : No

TE Code :

ACETAMINOPHEN

Johnson & Johnson

Dosage Form : SUPPOSITORY; RECTAL

Proprietary Name : TYLENOL

Dosage Strength : 120MG

Approval Date : 1982-01-01

Application Number : 17756

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
Web Link

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08

Brand Name : INJECTAPAP

Fi Europe 2024

Not Confirmed

Brand Name : INJECTAPAP

Fi Europe 2024

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RLD : No

TE Code :

ACETAMINOPHEN

McNeil Consumer Health

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : INJECTAPAP

Dosage Strength : 100MG/ML

Approval Date : 1986-03-07

Application Number : 17785

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
Web Link

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09

Brand Name : TYLENOL

Fi Europe 2024

Not Confirmed

Brand Name : TYLENOL

Fi Europe 2024

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RLD : Yes

TE Code :

ACETAMINOPHEN

Johnson & Johnson

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : TYLENOL

Dosage Strength : 650MG

Approval Date : 1994-06-08

Application Number : 19872

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

Product
Web Link

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10

Brand Name : TYLENOL

Fi Europe 2024

Not Confirmed

Brand Name : TYLENOL

Fi Europe 2024

Not Confirmed

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RLD : Yes

TE Code :

ACETAMINOPHEN

Johnson & Johnson

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : TYLENOL

Dosage Strength : 650MG

Approval Date : 2001-01-11

Application Number : 19872

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

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