14 Feb 2025
// FIERCE PHARMA
13 Feb 2025
// PRESS RELEASE
08 Feb 2025
// REUTERS
Latest Content by PharmaCompass
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01 3ACETAMINOPHEN; HYDROCODONE BITARTRATE
02 1ACYCLOVIR SODIUM
03 2ADALIMUMAB
04 1ALCAFTADINE
05 3ATOGEPANT
06 1ATROPINE
07 3ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE
08 1AVIBACTAM SODIUM; CEFTAZIDIME
09 1BERACTANT
10 4BIMATOPROST
11 1BIPERIDEN HYDROCHLORIDE
12 1BIPERIDEN LACTATE
13 2BRIMONIDINE TARTRATE
14 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE
15 2CALCITRIOL
16 1CARBIDOPA; LEVODOPA
17 4CARIPRAZINE HYDROCHLORIDE
18 3CARTEOLOL HYDROCHLORIDE
19 3CEFDINIR
20 2CEFTAROLINE FOSAMIL
21 2CHOLINE FENOFIBRATE
22 3CISATRACURIUM BESYLATE
23 4CITALOPRAM HYDROBROMIDE
24 8CLARITHROMYCIN
25 6CYCLOSPORINE
26 1DALBAVANCIN HYDROCHLORIDE
27 1DAPSONE
28 2DARIFENACIN HYDROBROMIDE
29 1DASABUVIR SODIUM; OMBITASVIR, PARITAPREVIR, RITONAVIR
30 1DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR
31 1DEOXYCHOLIC ACID
32 2DESERPIDINE
33 3DESERPIDINE; HYDROCHLOROTHIAZIDE
34 1DEXAMETHASONE
35 4DEXTROTHYROXINE SODIUM
36 3DICUMAROL
37 2DICYCLOMINE HYDROCHLORIDE
38 8DIVALPROEX SODIUM
39 4DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE
40 1DOXACURIUM CHLORIDE
41 2ELAGOLIX SODIUM
42 1ELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE; ELAGOLIX SODIUM
43 2ELUXADOLINE
44 3EPROSARTAN MESYLATE
45 2EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE
46 4ESCITALOPRAM OXALATE
47 4ESTRADIOL
48 4ETHCHLORVYNOL
49 1FAMOTIDINE
50 8FENOFIBRATE
51 2FLUOROMETHOLONE
52 1FOSCARBIDOPA; FOSLEVODOPA
53 1GATIFLOXACIN
54 2GLECAPREVIR; PIBRENTASVIR
55 1HEXOCYCLIUM METHYLSULFATE
56 2HYDROCHLOROTHIAZIDE
57 1HYDROCODONE BITARTRATE; IBUPROFEN
58 1IOPAMIDOL
59 2ISOPROTERENOL SULFATE
60 3KETOROLAC TROMETHAMINE
61 17LEUPROLIDE ACETATE
62 2LEUPROLIDE ACETATE; NORETHINDRONE ACETATE
63 4LEVOMILNACIPRAN HYDROCHLORIDE
64 12LEVOTHYROXINE SODIUM
65 3LINACLOTIDE
66 4LOPINAVIR; RITONAVIR
67 6MEMANTINE HYDROCHLORIDE
68 4MESALAMINE
69 1METHARBITAL
70 2METHYCLOTHIAZIDE
71 4MILNACIPRAN HYDROCHLORIDE
72 5MIVACURIUM CHLORIDE
73 1NALBUPHINE HYDROCHLORIDE
74 1NEBIVOLOL HYDROCHLORIDE; VALSARTAN
75 5NIACIN
76 1NITROGLYCERIN
77 1OMBITASVIR; PARITAPREVIR; RITONAVIR
78 1OXYBUTYNIN
79 1OXYBUTYNIN CHLORIDE
80 5PANCRELIPASE (AMYLASE;LIPASE;PROTEASE)
81 3PARAMETHADIONE
82 6PARICALCITOL
83 1PHENACEMIDE
84 1PILOCARPINE HYDROCHLORIDE
85 3POTASSIUM CHLORIDE
86 2PREDNISOLONE ACETATE
87 2PROGESTERONE
88 1PROTEIN HYDROLYSATE
89 3RISANKIZUMAB-RZAA
90 4RITONAVIR
91 1SEVOFLURANE
92 2SILODOSIN
93 1SODIUM NITROPRUSSIDE
94 2SUCRALFATE
95 1SULFADIAZINE
96 1SULFOXONE SODIUM
97 4TESTOSTERONE
98 3TRANDOLAPRIL
99 4TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE
100 1TRIAMCINOLONE ACETONIDE
101 3TRIMETHADIONE
102 2UBROGEPANT
103 4UPADACITINIB
104 1VALPROATE SODIUM
105 2VALPROIC ACID
106 3VENETOCLAX
107 3VILAZODONE HYDROCHLORIDE
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01 1AEROSOL, METERED;INHALATION
02 1CAPSULE, DELAYED REL PELLETS;ORAL
03 8CAPSULE, DELAYED RELEASE;ORAL
04 12CAPSULE, EXTENDED RELEASE;ORAL
05 31CAPSULE;ORAL
06 2EMULSION;OPHTHALMIC
07 9FILM, EXTENDED RELEASE;TRANSDERMAL
08 5FOR SUSPENSION;ORAL
09 1GEL;TOPICAL
10 1GEL;TRANSDERMAL
11 2GEL;VAGINAL
12 1IMPLANT;INTRAVITREAL
13 1IMPLANT;OPHTHALMIC
14 2INJECTABLE, TABLET;INTRAMUSCULAR, ORAL
15 1INJECTABLE; INJECTION
16 30INJECTABLE;INJECTION
17 1INJECTABLE;INTRAVENOUS
18 1LIQUID;INHALATION
19 1OINTMENT;INTRA-ANAL
20 1PELLETS;ORAL
21 2POWDER;INHALATION
22 8POWDER;INTRAMUSCULAR
23 4POWDER;INTRAVENOUS
24 1POWDER;ORAL
25 10SOLUTION/DROPS;OPHTHALMIC
26 1SOLUTION/DROPS;TOPICAL
27 1SOLUTION;INTRAMUSCULAR
28 6SOLUTION;INTRAVENOUS
29 1SOLUTION;OPHTHALMIC
30 7SOLUTION;ORAL
31 3SOLUTION;SUBCUTANEOUS
32 2SUPPOSITORY;RECTAL
33 4SUSPENSION/DROPS;OPHTHALMIC
34 1SUSPENSION;ENTERAL
35 1SUSPENSION;INTRATRACHEAL
36 1SUSPENSION;ORAL
37 1SYRINGE
38 1SYRUP;ORAL
39 5TABLET, DELAYED RELEASE;ORAL
40 2TABLET, EXTENDED RELEASE; ORAL
41 21TABLET, EXTENDED RELEASE;ORAL
42 93TABLET;ORAL
43 1VIAL
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01 10.001MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.002MG/ML (0.002MG/ML)
03 10.002MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 10.005MG/ML (0.005MG/ML)
05 10.01%
06 10.01MG/2ML (0.005MG/ML)
07 10.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
08 10.025MG/24HR
09 10.03%
10 10.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 20.05%
12 10.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
13 10.05MG/24HR
14 10.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
15 10.075MG/24HR
16 10.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
17 20.1%
18 10.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
19 10.12%
20 10.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
21 10.125MG;25MG
22 10.125MG;50MG
23 10.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
24 10.15%
25 10.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
26 10.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
27 10.1MG
28 10.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
29 10.1MG/24HR
30 10.1MG/INH
31 10.2%;EQ 0.5% BASE
32 20.25%
33 10.25MG
34 10.25MG;25MG
35 10.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
36 10.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
37 20.4%
38 10.45%
39 10.4MG/ML
40 10.4MG/ML;100MG/ML
41 10.4MG/ML;50MG/ML
42 10.4MG/ML;75MG/ML
43 20.5%
44 10.7MG
45 11%
46 11.25%
47 11.5MG/ML
48 110%
49 110% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 1100%
51 10100MG
52 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
53 1100MG/ML
54 1100MG/PACKET
55 1100MG;25MG
56 1100MG;40MG
57 110MCG
58 110MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
59 510MG
60 110MG/ML
61 110MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
62 110MG;14MG
63 110MG;21MG
64 110MG;28MG
65 110MG;7MG
66 311.25MG
67 111.25MG/VIAL,N/A;N/A,5MG
68 112.5MG
69 112.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 1120,000USP UNITS;24,000USP UNITS;76,000USP UNITS
71 1120MG/10ML;2400MG/10ML (12MG/ML;240MG/ML)
72 1125MG/5ML
73 1125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
74 1133.3MG;33.3MG
75 1134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
76 1145MCG
77 1145MG
78 114MG
79 114MG/2.8ML (1MG/0.2ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
80 115,000USP UNITS;3,000USP UNITS;9,500USP UNITS
81 2150MG
82 1150MG/ML
83 215MG
84 1160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
85 1165MG
86 1180,000USP UNITS;36,000USP UNITS;114,000USP UNITS
87 1187MG/5ML
88 21GM
89 11GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
90 11GM/10ML
91 11MCG
92 11MG
93 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
94 11MG/ML
95 11MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
96 12.5MG
97 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
98 12.5MG/24HR
99 1200MG
100 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
101 1200MG/5ML
102 1200MG;50MG
103 120MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
104 120MG
105 120MG/2ML (10MG/ML)
106 121MG
107 122.5MG
108 125%
109 2250MG
110 2250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
111 1250MG/5ML
112 2250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
113 525MG
114 125MG/ML
115 128MG
116 1290MCG
117 12MCG
118 22MG
119 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
120 12MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
121 12MG;180MG
122 12MG;240MG
123 23.75MG
124 13.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
125 13.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
126 13.75MG/VIAL,N/A;N/A,5MG
127 13.9MG/24HR
128 130,000USP UNITS;6,000USP UNITS;19,000USP UNITS
129 3300MG
130 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
131 1300MG/ML
132 430MG
133 1375MG
134 1375MG;500MG;750MG
135 14%
136 14.63MG/ML;20MG/ML
137 1400MG
138 1400MG/VIAL
139 140MG
140 240MG/0.8ML
141 345MG
142 148MG
143 14MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
144 24MG
145 14MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
146 14MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
147 14MG;240MG
148 25%
149 4500MG
150 4500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
151 1500MG;5MG
152 650MG
153 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
154 150MG;20MG/PACKET
155 154MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
156 25MG
157 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
158 15MG/24HR
159 15MG/ML
160 160,000USP UNITS;12,000USP UNITS;38,000USP UNITS
161 2600MG/VIAL
162 1600MG;12.5MG
163 1600MG;25MG
164 160MG
165 161%
166 1660MG;10MG
167 167MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
168 16MG
169 27.5MG
170 17.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
171 17.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
172 172MCG
173 1750MG
174 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
175 1750MG;7.5MG
176 175MG
177 175MG/0.83ML
178 17MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
179 18%
180 1800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
181 180MG/ML
182 180MG/ML;20MG/ML
183 18MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
184 18MG
185 1EQ 0.5GM BASE;2GM/VIAL
186 1EQ 0.5MG BASE/ML
187 1EQ 1.5MG BASE
188 1EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
189 2EQ 10MG BASE
190 1EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
191 1EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
192 1EQ 120MG BASE
193 2EQ 125MG VALPROIC ACID
194 1EQ 135MG FENOFIBRIC ACID
195 1EQ 150MG BASE
196 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
197 1EQ 1MG BASE/ML
198 1EQ 200MG BASE
199 1EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
200 3EQ 20MG BASE
201 1EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
202 1EQ 250MG BASE;12.5MG, 75MG, 50MG
203 2EQ 250MG VALPROIC ACID
204 1EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
205 2EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
206 1EQ 2MG SULFATE/0.7ML
207 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
208 1EQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE
209 1EQ 3MG BASE
210 1EQ 4.5MG BASE
211 1EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
212 2EQ 40MG BASE
213 1EQ 45MG FENOFIBRIC ACID
214 1EQ 500MG BASE/VIAL
215 2EQ 500MG VALPROIC ACID
216 1EQ 50MG BASE/100ML
217 1EQ 50MG BASE/ML
218 1EQ 5MG BASE
219 1EQ 5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
220 1EQ 5MG BASE;80MG
221 1EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
222 1EQ 60MG BASE
223 1EQ 6MG BASE
224 1EQ 7.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
225 1EQ 80MG BASE
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01 142DISCN
02 2OTC
03 129RX
04 16Blank
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : VICODIN HP
Dosage Strength : 660MG;10MG
Approval Date : 1996-09-23
Application Number : 40117
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : VICODIN
Dosage Strength : 500MG;5MG
Approval Date : 1983-01-07
Application Number : 88058
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : VICODIN ES
Dosage Strength : 750MG;7.5MG
Approval Date : 1988-12-09
Application Number : 89736
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : ACYCLOVIR
Dosage Strength : EQ 50MG BASE/ML
Approval Date : 1999-07-26
Application Number : 75114
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD :
TE Code :
Dosage Form : SYRINGE
Proprietary Name : HUMIRA
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 125057
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : VIAL
Proprietary Name : HUMIRA
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 125057
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : LASTACAFT
Dosage Strength : 0.25%
Approval Date : 2010-07-28
Application Number : 22134
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : QULIPTA
Dosage Strength : 10MG
Approval Date : 2021-09-28
Application Number : 215206
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : QULIPTA
Dosage Strength : 30MG
Approval Date : 2021-09-28
Application Number : 215206
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : QULIPTA
Dosage Strength : 60MG
Approval Date : 2021-09-28
Application Number : 215206
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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