18 Nov 2024
// PR NEWSWIRE
18 Nov 2024
// FIERCE PHARMA
18 Nov 2024
// FIERCE PHARMA
Latest Content by PharmaCompass
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 AND 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 1PROTEIN HYDROLYSATE
88 3RISANKIZUMAB-RZAA
89 4RITONAVIR
90 1SEVOFLURANE
91 1SODIUM NITROPRUSSIDE
92 2SUCRALFATE
93 1SULFADIAZINE
94 1SULFOXONE SODIUM
95 4TESTOSTERONE
96 3TRANDOLAPRIL
97 4TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE
98 1TRIAMCINOLONE ACETONIDE
99 3TRIMETHADIONE
100 2UBROGEPANT
101 4UPADACITINIB
102 1VALPROATE SODIUM
103 2VALPROIC ACID
104 3VENETOCLAX
105 3VILAZODONE HYDROCHLORIDE
01 1AEROSOL, METERED;INHALATION
02 1CAPSULE, DELAYED REL PELLETS;ORAL
03 8CAPSULE, DELAYED RELEASE;ORAL
04 12CAPSULE, EXTENDED RELEASE;ORAL
05 29CAPSULE;ORAL
06 2EMULSION;OPHTHALMIC
07 9FILM, EXTENDED RELEASE;TRANSDERMAL
08 5FOR SUSPENSION;ORAL
09 1GEL;TOPICAL
10 1GEL;TRANSDERMAL
11 1IMPLANT;INTRAVITREAL
12 1IMPLANT;OPHTHALMIC
13 2INJECTABLE, TABLET;INTRAMUSCULAR, ORAL
14 1INJECTABLE; INJECTION
15 30INJECTABLE;INJECTION
16 1INJECTABLE;INTRAVENOUS
17 1INJECTION;SOLUTION
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 2SOLUTION;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
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 210MG/ML
61 110MG;14MG
62 110MG;21MG
63 110MG;28MG
64 110MG;7MG
65 311.25MG
66 111.25MG/VIAL,N/A;N/A,5MG
67 112.5MG
68 112.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
69 1120,000USP UNITS;24,000USP UNITS;76,000USP UNITS
70 1125MG/5ML
71 1125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
72 112MG/240MG / ML
73 1133.3MG;33.3MG
74 1134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
75 1145MCG
76 1145MG
77 114MG
78 114MG/2.8ML (1MG/0.2ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
79 115,000USP UNITS;3,000USP UNITS;9,500USP UNITS
80 2150MG
81 1150MG/ML
82 215MG
83 1160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
84 1165MG
85 1180,000USP UNITS;36,000USP UNITS;114,000USP UNITS
86 1187MG/5ML
87 21GM
88 11GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
89 11GM/10ML
90 11MCG
91 11MG
92 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
93 11MG/ML
94 11MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
95 12.5MG
96 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
97 12.5MG/24HR
98 1200MG
99 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
100 1200MG/5ML
101 1200MG;50MG
102 120MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
103 120MG
104 120MG/2ML (10MG/ML)
105 121MG
106 122.5MG
107 125%
108 2250MG
109 2250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
110 1250MG/5ML
111 2250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
112 525MG
113 125MG/ML
114 128MG
115 1290MCG
116 12MCG
117 22MG
118 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
119 12MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
120 12MG;180MG
121 12MG;240MG
122 23.75MG
123 13.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
124 13.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
125 13.75MG/VIAL,N/A;N/A,5MG
126 13.9MG/24HR
127 130,000USP UNITS;6,000USP UNITS;19,000USP UNITS
128 3300MG
129 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
130 1300MG/ML
131 430MG
132 1375MG
133 1375MG;500MG;750MG
134 14.63MG/ML;20MG/ML
135 1400MG
136 1400MG/VIAL
137 140MG
138 240MG/0.8ML
139 345MG
140 148MG
141 14MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
142 14MG
143 14MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
144 14MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
145 14MG;240MG
146 25%
147 4500MG
148 4500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
149 1500MG;5MG
150 650MG
151 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
152 150MG;20MG/PACKET
153 154MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
154 25MG
155 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
156 15MG/24HR
157 15MG/ML
158 160,000USP UNITS;12,000USP UNITS;38,000USP UNITS
159 2600MG/VIAL
160 1600MG;12.5MG
161 1600MG;25MG
162 160MG
163 161%
164 1660MG;10MG
165 167MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
166 16MG
167 27.5MG
168 17.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
169 17.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
170 172MCG
171 1750MG
172 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
173 1750MG;7.5MG
174 175MG
175 175MG/0.83ML
176 17MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
177 1800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
178 180MG/ML
179 180MG/ML;20MG/ML
180 18MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
181 1EQ 0.5GM BASE;2GM/VIAL
182 1EQ 0.5MG BASE/ML
183 1EQ 1.5MG BASE
184 1EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
185 2EQ 10MG BASE
186 1EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
187 1EQ 10MG BASE/ML
188 1EQ 120MG BASE
189 2EQ 125MG VALPROIC ACID
190 1EQ 135MG FENOFIBRIC ACID
191 1EQ 150MG BASE
192 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
193 1EQ 1MG BASE/ML
194 1EQ 200MG BASE
195 1EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
196 3EQ 20MG BASE
197 1EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
198 1EQ 250MG BASE;12.5MG, 75MG, 50MG
199 2EQ 250MG VALPROIC ACID
200 2EQ 2MG BASE/ML
201 1EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
202 1EQ 2MG SULFATE/0.7ML
203 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
204 1EQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE
205 1EQ 3MG BASE
206 1EQ 4.5MG BASE
207 1EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
208 2EQ 40MG BASE
209 1EQ 45MG FENOFIBRIC ACID
210 1EQ 500MG BASE/VIAL
211 2EQ 500MG VALPROIC ACID
212 1EQ 50MG BASE/100ML
213 1EQ 50MG BASE/ML
214 1EQ 5MG BASE
215 1EQ 5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
216 1EQ 5MG BASE;80MG
217 1EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
218 1EQ 60MG BASE
219 1EQ 6MG BASE
220 1EQ 7.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
221 1EQ 80MG BASE
01 141DISCN
02 2OTC
03 125RX
04 17Blank
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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