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Approved Drug Products of Abbvie Inc listed in the FDA Orange Book. Original Data : FDA Website

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01 ACETAMINOPHEN; HYDROCODONE BITARTRATE (3)

02 ACYCLOVIR SODIUM (1)

03 ADALIMUMAB (2)

04 ALCAFTADINE (1)

05 ATOGEPANT (3)

06 ATROPINE (1)

07 ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE (3)

08 BERACTANT (1)

09 BIMATOPROST (4)

10 BIPERIDEN HYDROCHLORIDE (1)

11 BIPERIDEN LACTATE (1)

12 BRIMONIDINE TARTRATE (2)

13 BRIMONIDINE TARTRATE; TIMOLOL MALEATE (1)

14 CALCITRIOL (2)

15 CARBIDOPA; LEVODOPA (1)

16 CARIPRAZINE HYDROCHLORIDE (4)

17 CARTEOLOL HYDROCHLORIDE (3)

18 CEFDINIR (3)

19 CEFTAROLINE FOSAMIL (2)

20 CHOLINE FENOFIBRATE (2)

21 CISATRACURIUM BESYLATE (3)

22 CITALOPRAM HYDROBROMIDE (4)

23 CLARITHROMYCIN (8)

24 CYCLOSPORINE (6)

25 DALBAVANCIN HYDROCHLORIDE (1)

26 DAPSONE (1)

27 DARIFENACIN HYDROBROMIDE (2)

28 DASABUVIR SODIUM; OMBITASVIR, PARITAPREVIR, RITONAVIR (1)

29 DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR (1)

30 DEOXYCHOLIC ACID (1)

31 DESERPIDINE (2)

32 DESERPIDINE; HYDROCHLOROTHIAZIDE (3)

33 DEXAMETHASONE (1)

34 DEXTROTHYROXINE SODIUM (4)

35 DICUMAROL (3)

36 DICYCLOMINE HYDROCHLORIDE (2)

37 DIVALPROEX SODIUM (8)

38 DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE (4)

39 DOXACURIUM CHLORIDE (1)

40 ELAGOLIX SODIUM (2)

41 ELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE; ELAGOLIX SODIUM (1)

42 ELUXADOLINE (2)

43 EPROSARTAN MESYLATE (3)

44 EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE (2)

45 ESCITALOPRAM OXALATE (4)

46 ESTRADIOL (4)

47 ETHCHLORVYNOL (4)

48 FAMOTIDINE (1)

49 FENOFIBRATE (8)

50 FLUOROMETHOLONE (2)

51 GATIFLOXACIN (1)

52 GLECAPREVIR; PIBRENTASVIR (2)

53 HEXOCYCLIUM METHYLSULFATE (1)

54 HYDROCHLOROTHIAZIDE (2)

55 HYDROCODONE BITARTRATE; IBUPROFEN (1)

56 IOPAMIDOL (1)

57 ISOPROTERENOL SULFATE (2)

58 KETOROLAC TROMETHAMINE (3)

59 LEUPROLIDE ACETATE (17)

60 LEUPROLIDE ACETATE; NORETHINDRONE ACETATE (2)

61 LEVOMILNACIPRAN HYDROCHLORIDE (4)

62 LEVOTHYROXINE SODIUM (12)

63 LINACLOTIDE (3)

64 LOPINAVIR; RITONAVIR (4)

65 MEMANTINE HYDROCHLORIDE (6)

66 MESALAMINE (4)

67 METHARBITAL (1)

68 METHYCLOTHIAZIDE (2)

69 MILNACIPRAN HYDROCHLORIDE (4)

70 MIVACURIUM CHLORIDE (5)

71 NALBUPHINE HYDROCHLORIDE (1)

72 NEBIVOLOL HYDROCHLORIDE; VALSARTAN (1)

73 NIACIN (5)

74 NITROGLYCERIN (1)

75 OMBITASVIR; PARITAPREVIR; RITONAVIR (1)

76 OXYBUTYNIN (1)

77 OXYBUTYNIN CHLORIDE (1)

78 PANCRELIPASE (AMYLASE;LIPASE;PROTEASE) (5)

79 PARAMETHADIONE (3)

80 PARICALCITOL (6)

81 PHENACEMIDE (1)

82 PILOCARPINE HYDROCHLORIDE (1)

83 POTASSIUM CHLORIDE (3)

84 PREDNISOLONE ACETATE (2)

85 PROTEIN HYDROLYSATE (1)

86 RISANKIZUMAB-RZAA (3)

87 RITONAVIR (4)

88 SEVOFLURANE (1)

89 SODIUM NITROPRUSSIDE (1)

90 SUCRALFATE (2)

91 SULFADIAZINE (1)

92 SULFOXONE SODIUM (1)

93 TESTOSTERONE (4)

94 TRANDOLAPRIL (3)

95 TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE (4)

96 TRIAMCINOLONE ACETONIDE (1)

97 TRIMETHADIONE (3)

98 UBROGEPANT (2)

99 UPADACITINIB (7)

100 VALPROATE SODIUM (1)

101 VALPROIC ACID (2)

102 VENETOCLAX (3)

103 VILAZODONE HYDROCHLORIDE (3)

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01 AEROSOL, METERED;INHALATION (1)

02 CAPSULE, DELAYED REL PELLETS;ORAL (1)

03 CAPSULE, DELAYED RELEASE;ORAL (8)

04 CAPSULE, EXTENDED RELEASE;ORAL (12)

05 CAPSULE;ORAL (29)

06 EMULSION;OPHTHALMIC (2)

07 FILM, EXTENDED RELEASE;TRANSDERMAL (9)

08 FOR SUSPENSION;ORAL (5)

09 GEL;TOPICAL (1)

10 GEL;TRANSDERMAL (1)

11 IMPLANT;INTRAVITREAL (1)

12 IMPLANT;OPHTHALMIC (1)

13 INJECTABLE, TABLET;INTRAMUSCULAR, ORAL (2)

14 INJECTABLE; INJECTION (1)

15 INJECTABLE;INJECTION (31)

16 INJECTABLE;INTRAVENOUS (1)

17 LIQUID;INHALATION (1)

18 OINTMENT;INTRA-ANAL (1)

19 PELLETS;ORAL (1)

20 POWDER;INHALATION (2)

21 POWDER;INTRAMUSCULAR (8)

22 POWDER;INTRAVENOUS (3)

23 POWDER;ORAL (1)

24 SOLUTION/DROPS;OPHTHALMIC (10)

25 SOLUTION/DROPS;TOPICAL (1)

26 SOLUTION;INTRAMUSCULAR (1)

27 SOLUTION;INTRAVENOUS (6)

28 SOLUTION;OPHTHALMIC (1)

29 SOLUTION;ORAL (7)

30 SOLUTION;SUBCUTANEOUS (1)

31 SUPPOSITORY;RECTAL (2)

32 SUSPENSION/DROPS;OPHTHALMIC (4)

33 SUSPENSION;ENTERAL (1)

34 SUSPENSION;INTRATRACHEAL (1)

35 SUSPENSION;ORAL (1)

36 SYRINGE (1)

37 SYRUP;ORAL (1)

38 TABLET, DELAYED RELEASE;ORAL (5)

39 TABLET, EXTENDED RELEASE; ORAL (2)

40 TABLET, EXTENDED RELEASE;ORAL (24)

41 TABLET;ORAL (93)

42 VIAL (1)

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01 0.001MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

02 0.002MG/ML (0.002MG/ML) (1)

03 0.002MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

04 0.005MG/ML (0.005MG/ML) (1)

05 0.01% (1)

06 0.01MG/2ML (0.005MG/ML) (1)

07 0.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

08 0.025MG/24HR (1)

09 0.03% (1)

10 0.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

11 0.05% (2)

12 0.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

13 0.05MG/24HR (1)

14 0.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

15 0.075MG/24HR (1)

16 0.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

17 0.1% (2)

18 0.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

19 0.12% (1)

20 0.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

21 0.125MG;25MG (1)

22 0.125MG;50MG (1)

23 0.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

24 0.15% (1)

25 0.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

26 0.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

27 0.1MG (1)

28 0.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

29 0.1MG/24HR (1)

30 0.1MG/INH (1)

31 0.2%;EQ 0.5% BASE (1)

32 0.25% (2)

33 0.25MG (1)

34 0.25MG;25MG (1)

35 0.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

36 0.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

37 0.4% (2)

38 0.45% (1)

39 0.4MG/ML (1)

40 0.4MG/ML;100MG/ML (1)

41 0.4MG/ML;50MG/ML (1)

42 0.4MG/ML;75MG/ML (1)

43 0.5% (2)

44 0.7MG (1)

45 1% (1)

46 1.25% (1)

47 1.5MG/ML (1)

48 10% (1)

49 10% (100MG/PACKET) (1)

50 100% (1)

51 100MG (10)

52 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

53 100MG/ML (1)

54 100MG/PACKET (1)

55 100MG;25MG (1)

56 100MG;40MG (1)

57 10MCG (1)

58 10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

59 10MG (5)

60 10MG/ML (2)

61 10MG;14MG (1)

62 10MG;21MG (1)

63 10MG;28MG (1)

64 10MG;7MG (1)

65 11.25MG (3)

66 11.25MG/VIAL,N/A;N/A,5MG (1)

67 12.5MG (1)

68 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

69 120,000USP UNITS;24,000USP UNITS;76,000USP UNITS (1)

70 125MG/5ML (1)

71 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

72 133.3MG;33.3MG (1)

73 134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

74 145MCG (1)

75 145MG (1)

76 14MG (1)

77 15,000USP UNITS;3,000USP UNITS;9,500USP UNITS (1)

78 150MG (2)

79 150MG/ML (1)

80 15MG (3)

81 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

82 165MG (1)

83 180,000USP UNITS;36,000USP UNITS;114,000USP UNITS (1)

84 187MG/5ML (1)

85 1GM (2)

86 1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

87 1GM/10ML (1)

88 1MCG (1)

89 1MG (1)

90 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

91 1MG/0.2ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

92 1MG/ML (1)

93 1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

94 2.5MG (1)

95 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

96 2.5MG/24HR (1)

97 200MG (1)

98 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

99 200MG/5ML (1)

100 200MG;50MG (1)

101 20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

102 20MG (1)

103 20MG/2ML (10MG/ML) (1)

104 21MG (1)

105 22.5MG (1)

106 25% (1)

107 250MG (2)

108 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

109 250MG/5ML (1)

110 250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

111 25MG (5)

112 25MG/ML (1)

113 28MG (1)

114 290MCG (1)

115 2MCG (1)

116 2MG (2)

117 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

118 2MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

119 2MG;180MG (1)

120 2MG;240MG (1)

121 3.75MG (2)

122 3.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

123 3.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

124 3.75MG/VIAL,N/A;N/A,5MG (1)

125 3.9MG/24HR (1)

126 30,000USP UNITS;6,000USP UNITS;19,000USP UNITS (1)

127 300MG (3)

128 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

129 300MG/ML (1)

130 30MG (5)

131 375MG (1)

132 375MG;500MG;750MG (1)

133 4.63MG/ML;20MG/ML (1)

134 400MG (1)

135 400MG/VIAL (1)

136 40MG (1)

137 40MG/0.8ML (2)

138 45MG (4)

139 48MG (1)

140 4MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

141 4MG (1)

142 4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

143 4MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

144 4MG;240MG (1)

145 5% (2)

146 500MG (4)

147 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (4)

148 500MG;5MG (1)

149 50MG (6)

150 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

151 50MG;20MG/PACKET (1)

152 54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

153 5MG (2)

154 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

155 5MG/24HR (1)

156 5MG/ML (1)

157 60,000USP UNITS;12,000USP UNITS;38,000USP UNITS (1)

158 600MG/VIAL (2)

159 600MG;12.5MG (1)

160 600MG;25MG (1)

161 60MG (1)

162 61% (1)

163 660MG;10MG (1)

164 67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

165 6MG (1)

166 7.5MG (2)

167 7.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

168 7.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

169 72MCG (1)

170 750MG (1)

171 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

172 750MG;7.5MG (1)

173 75MG (1)

174 75MG/0.83ML (1)

175 7MG (1)

176 800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

177 80MG/ML (1)

178 80MG/ML;20MG/ML (1)

179 8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

180 EQ 0.5MG BASE/ML (1)

181 EQ 1.5MG BASE (1)

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

183 EQ 10MG BASE (2)

184 EQ 10MG BASE/5ML (EQ 2MG BASE/ML) (1)

185 EQ 10MG BASE/ML (1)

186 EQ 120MG BASE (1)

187 EQ 125MG VALPROIC ACID (2)

188 EQ 135MG FENOFIBRIC ACID (1)

189 EQ 150MG BASE (1)

190 EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

191 EQ 1MG BASE/ML (1)

192 EQ 200MG BASE (1)

193 EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

194 EQ 20MG BASE (3)

195 EQ 20MG BASE/10ML (EQ 2MG BASE/ML) (1)

196 EQ 250MG BASE;12.5MG, 75MG, 50MG (1)

197 EQ 250MG VALPROIC ACID (2)

198 EQ 2MG BASE/ML (2)

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

200 EQ 2MG SULFATE/0.7ML (1)

201 EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

202 EQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE (1)

203 EQ 3MG BASE (1)

204 EQ 4.5MG BASE (1)

205 EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

206 EQ 40MG BASE (2)

207 EQ 45MG FENOFIBRIC ACID (1)

208 EQ 500MG BASE/VIAL (1)

209 EQ 500MG VALPROIC ACID (2)

210 EQ 50MG BASE/100ML (1)

211 EQ 50MG BASE/ML (1)

212 EQ 5MG BASE (1)

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

214 EQ 5MG BASE;80MG (1)

215 EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

216 EQ 60MG BASE (1)

217 EQ 6MG BASE (1)

218 EQ 7.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

219 EQ 80MG BASE (1)

filter

01 DISCN (136)

02 OTC (2)

03 RX (129)

04 Blank (19)

URL Supplier Web Content
TABLET; ORAL
660MG;10MG
1996-09-23
40117
VICODIN HP
DISCN
No
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
500MG;5MG
1983-01-07
88058
VICODIN
DISCN
No
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
750MG;7.5MG
1988-12-09
89736
VICODIN ES
DISCN
No
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
INJECTABLE; INJECT...
EQ 50MG BASE/ML
1999-07-26
75114
ACYCLOVIR
DISCN
No
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
SYRINGE
40MG/0.8ML
125057
HUMIRA
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
VIAL
40MG/0.8ML
125057
HUMIRA
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
SOLUTION/DROPS; OP...
0.25%
2010-07-28
22134
LASTACAFT
OTC
Yes
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
10MG
2021-09-28
215206
QULIPTA
RX
Yes
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
30MG
2021-09-28
215206
QULIPTA
RX
Yes
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
60MG
2021-09-28
215206
QULIPTA
RX
Yes
Abbvie Company Banner

IPS 2024

Not Confirmed

envelop Contact Supplier
Post Enquiry
POST ENQUIRY