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31 Mar 2025
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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; AZTREONAM
09 1AVIBACTAM SODIUM; CEFTAZIDIME
10 1BERACTANT
11 4BIMATOPROST
12 1BIPERIDEN HYDROCHLORIDE
13 1BIPERIDEN LACTATE
14 2BRIMONIDINE TARTRATE
15 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE
16 2CALCITRIOL
17 1CARBIDOPA; LEVODOPA
18 4CARIPRAZINE HYDROCHLORIDE
19 3CARTEOLOL HYDROCHLORIDE
20 3CEFDINIR
21 2CEFTAROLINE FOSAMIL
22 2CHOLINE FENOFIBRATE
23 3CISATRACURIUM BESYLATE
24 4CITALOPRAM HYDROBROMIDE
25 8CLARITHROMYCIN
26 6CYCLOSPORINE
27 1DALBAVANCIN HYDROCHLORIDE
28 1DAPSONE
29 2DARIFENACIN HYDROBROMIDE
30 1DASABUVIR SODIUM; OMBITASVIR, PARITAPREVIR, RITONAVIR
31 1DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR
32 1DEOXYCHOLIC ACID
33 2DESERPIDINE
34 3DESERPIDINE; HYDROCHLOROTHIAZIDE
35 1DEXAMETHASONE
36 4DEXTROTHYROXINE SODIUM
37 3DICUMAROL
38 2DICYCLOMINE HYDROCHLORIDE
39 8DIVALPROEX SODIUM
40 4DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE
41 1DOXACURIUM CHLORIDE
42 1EFLORNITHINE HYDROCHLORIDE
43 2ELAGOLIX SODIUM
44 1ELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE; ELAGOLIX SODIUM
45 2ELUXADOLINE
46 3EPROSARTAN MESYLATE
47 2EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE
48 4ESCITALOPRAM OXALATE
49 4ESTRADIOL
50 4ETHCHLORVYNOL
51 1FAMOTIDINE
52 8FENOFIBRATE
53 2FLUOROMETHOLONE
54 1FOSCARBIDOPA; FOSLEVODOPA
55 1GATIFLOXACIN
56 2GLECAPREVIR; PIBRENTASVIR
57 1HEXOCYCLIUM METHYLSULFATE
58 2HYDROCHLOROTHIAZIDE
59 1HYDROCODONE BITARTRATE; IBUPROFEN
60 1IOPAMIDOL
61 2ISOPROTERENOL SULFATE
62 3KETOROLAC TROMETHAMINE
63 17LEUPROLIDE ACETATE
64 2LEUPROLIDE ACETATE; NORETHINDRONE ACETATE
65 4LEVOMILNACIPRAN HYDROCHLORIDE
66 12LEVOTHYROXINE SODIUM
67 3LINACLOTIDE
68 4LOPINAVIR; RITONAVIR
69 6MEMANTINE HYDROCHLORIDE
70 4MESALAMINE
71 1METHARBITAL
72 2METHYCLOTHIAZIDE
73 4MILNACIPRAN HYDROCHLORIDE
74 5MIVACURIUM CHLORIDE
75 1NALBUPHINE HYDROCHLORIDE
76 1NEBIVOLOL HYDROCHLORIDE; VALSARTAN
77 5NIACIN
78 1NITROGLYCERIN
79 1OMBITASVIR; PARITAPREVIR; RITONAVIR
80 1OXYBUTYNIN
81 1OXYBUTYNIN CHLORIDE
82 5PANCRELIPASE (AMYLASE;LIPASE;PROTEASE)
83 3PARAMETHADIONE
84 6PARICALCITOL
85 1PHENACEMIDE
86 1PILOCARPINE HYDROCHLORIDE
87 3POTASSIUM CHLORIDE
88 2PREDNISOLONE ACETATE
89 2PROGESTERONE
90 1PROTEIN HYDROLYSATE
91 3RISANKIZUMAB-RZAA
92 4RITONAVIR
93 1SEVOFLURANE
94 2SILODOSIN
95 1SODIUM NITROPRUSSIDE
96 2SUCRALFATE
97 1SULFADIAZINE
98 1SULFOXONE SODIUM
99 4TESTOSTERONE
100 3TRANDOLAPRIL
101 4TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE
102 1TRIAMCINOLONE ACETONIDE
103 3TRIMETHADIONE
104 2UBROGEPANT
105 4UPADACITINIB
106 1VALPROATE SODIUM
107 2VALPROIC ACID
108 3VENETOCLAX
109 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 1CREAM;TOPICAL
07 2EMULSION;OPHTHALMIC
08 9FILM, EXTENDED RELEASE;TRANSDERMAL
09 5FOR SUSPENSION;ORAL
10 1GEL;TOPICAL
11 1GEL;TRANSDERMAL
12 2GEL;VAGINAL
13 1IMPLANT;INTRAVITREAL
14 1IMPLANT;OPHTHALMIC
15 2INJECTABLE, TABLET;INTRAMUSCULAR, ORAL
16 1INJECTABLE; INJECTION
17 30INJECTABLE;INJECTION
18 1INJECTABLE;INTRAVENOUS
19 1LIQUID;INHALATION
20 1OINTMENT;INTRA-ANAL
21 1PELLETS;ORAL
22 2POWDER;INHALATION
23 8POWDER;INTRAMUSCULAR
24 5POWDER;INTRAVENOUS
25 1POWDER;ORAL
26 10SOLUTION/DROPS;OPHTHALMIC
27 1SOLUTION/DROPS;TOPICAL
28 1SOLUTION;INTRAMUSCULAR
29 6SOLUTION;INTRAVENOUS
30 1SOLUTION;OPHTHALMIC
31 7SOLUTION;ORAL
32 3SOLUTION;SUBCUTANEOUS
33 2SUPPOSITORY;RECTAL
34 4SUSPENSION/DROPS;OPHTHALMIC
35 1SUSPENSION;ENTERAL
36 1SUSPENSION;INTRATRACHEAL
37 1SUSPENSION;ORAL
38 1SYRINGE
39 1SYRUP;ORAL
40 5TABLET, DELAYED RELEASE;ORAL
41 2TABLET, EXTENDED RELEASE; ORAL
42 21TABLET, EXTENDED RELEASE;ORAL
43 93TABLET;ORAL
44 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**
74 113.9%
75 1133.3MG;33.3MG
76 1134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
77 1145MCG
78 1145MG
79 114MG
80 114MG/2.8ML (1MG/0.2ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
81 115,000USP UNITS;3,000USP UNITS;9,500USP UNITS
82 2150MG
83 1150MG/ML
84 215MG
85 1160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
86 1165MG
87 1180,000USP UNITS;36,000USP UNITS;114,000USP UNITS
88 1187MG/5ML
89 21GM
90 11GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
91 11GM/10ML
92 11MCG
93 11MG
94 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
95 11MG/ML
96 11MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
97 12.5MG
98 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
99 12.5MG/24HR
100 1200MG
101 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
102 1200MG/5ML
103 1200MG;50MG
104 120MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
105 120MG
106 120MG/2ML (10MG/ML)
107 121MG
108 122.5MG
109 125%
110 2250MG
111 2250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
112 1250MG/5ML
113 2250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
114 525MG
115 125MG/ML
116 128MG
117 1290MCG
118 12MCG
119 22MG
120 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
121 12MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
122 12MG;180MG
123 12MG;240MG
124 23.75MG
125 13.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
126 13.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
127 13.75MG/VIAL,N/A;N/A,5MG
128 13.9MG/24HR
129 130,000USP UNITS;6,000USP UNITS;19,000USP UNITS
130 3300MG
131 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
132 1300MG/ML
133 430MG
134 1375MG
135 1375MG;500MG;750MG
136 14%
137 14.63MG/ML;20MG/ML
138 1400MG
139 1400MG/VIAL
140 140MG
141 240MG/0.8ML
142 345MG
143 148MG
144 14MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
145 24MG
146 14MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
147 14MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
148 14MG;240MG
149 25%
150 4500MG
151 4500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
152 1500MG;5MG
153 650MG
154 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
155 150MG;20MG/PACKET
156 154MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
157 25MG
158 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
159 15MG/24HR
160 15MG/ML
161 160,000USP UNITS;12,000USP UNITS;38,000USP UNITS
162 2600MG/VIAL
163 1600MG;12.5MG
164 1600MG;25MG
165 160MG
166 161%
167 1660MG;10MG
168 167MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
169 16MG
170 27.5MG
171 17.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
172 17.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
173 172MCG
174 1750MG
175 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
176 1750MG;7.5MG
177 175MG
178 175MG/0.83ML
179 17MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
180 18%
181 1800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
182 180MG/ML
183 180MG/ML;20MG/ML
184 18MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
185 18MG
186 1EQ 0.5GM BASE/VIAL;1.5GM/VIAL
187 1EQ 0.5GM BASE;2GM/VIAL
188 1EQ 0.5MG BASE/ML
189 1EQ 1.5MG BASE
190 1EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
191 2EQ 10MG BASE
192 1EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
193 1EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
194 1EQ 120MG BASE
195 2EQ 125MG VALPROIC ACID
196 1EQ 135MG FENOFIBRIC ACID
197 1EQ 150MG BASE
198 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
199 1EQ 1MG BASE/ML
200 1EQ 200MG BASE
201 1EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
202 3EQ 20MG BASE
203 1EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
204 1EQ 250MG BASE;12.5MG, 75MG, 50MG
205 2EQ 250MG VALPROIC ACID
206 1EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
207 2EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
208 1EQ 2MG SULFATE/0.7ML
209 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
210 1EQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE
211 1EQ 3MG BASE
212 1EQ 4.5MG BASE
213 1EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
214 2EQ 40MG BASE
215 1EQ 45MG FENOFIBRIC ACID
216 1EQ 500MG BASE/VIAL
217 2EQ 500MG VALPROIC ACID
218 1EQ 50MG BASE/100ML
219 1EQ 50MG BASE/ML
220 1EQ 5MG BASE
221 1EQ 5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
222 1EQ 5MG BASE;80MG
223 1EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
224 1EQ 60MG BASE
225 1EQ 6MG BASE
226 1EQ 7.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
227 1EQ 80MG BASE
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01 144DISCN
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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