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01 2ACETAZOLAMIDE
02 2AMINOCAPROIC ACID
03 3BACLOFEN
04 3BUMETANIDE
05 5CHLORPROMAZINE HYDROCHLORIDE
06 2CHLORTHALIDONE
07 1CLINDAMYCIN PALMITATE HYDROCHLORIDE
08 1CLOMIPHENE CITRATE
09 1CYPROHEPTADINE HYDROCHLORIDE
10 5DOXEPIN HYDROCHLORIDE
11 2GLYCOPYRROLATE
12 4HYDROXYCHLOROQUINE SULFATE
13 3IRBESARTAN
14 4LABETALOL HYDROCHLORIDE
15 2METRONIDAZOLE
16 2MODAFINIL
17 1NITROFURANTOIN
18 4PERPHENAZINE
19 3PRAZOSIN HYDROCHLORIDE
20 2RANITIDINE HYDROCHLORIDE
21 3SERTRALINE HYDROCHLORIDE
22 3SILDENAFIL CITRATE
23 1VALGANCICLOVIR HYDROCHLORIDE
24 2VENLAFAXINE HYDROCHLORIDE
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01 10CAPSULE;ORAL
02 2FOR SOLUTION;ORAL
03 1SUSPENSION;ORAL
04 2TABLET, EXTENDED RELEASE;ORAL
05 46TABLET;ORAL
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01 10.5MG
02 4100MG
03 210MG
04 1125MG
05 1150MG
06 116MG
07 11GM
08 21MG
09 4200MG
10 120MG
11 2250MG
12 225MG
13 125MG/5ML
14 32MG
15 3300MG
16 2400MG
17 24MG
18 2500MG
19 350MG
20 150MG/ML
21 15MG
22 175MG
23 18MG
24 3EQ 100MG BASE
25 1EQ 10MG BASE
26 2EQ 150MG BASE
27 1EQ 1MG BASE
28 1EQ 225MG BASE
29 3EQ 25MG BASE
30 1EQ 2MG BASE
31 1EQ 300MG BASE
32 3EQ 50MG BASE
33 1EQ 5MG BASE
34 1EQ 75MG BASE
35 1EQ 75MG BASE/5ML
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01 10DISCN
02 51RX
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAZOLAMIDE
Dosage Strength : 125MG
Approval Date : 2021-02-22
Application Number : 211372
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAZOLAMIDE
Dosage Strength : 250MG
Approval Date : 2021-02-22
Application Number : 211372
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMINOCAPROIC ACID
Dosage Strength : 500MG
Approval Date : 2022-09-14
Application Number : 213944
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : AMINOCAPROIC ACID
Dosage Strength : 1GM
Approval Date : 2022-09-14
Application Number : 213944
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BACLOFEN
Dosage Strength : 10MG
Approval Date : 2010-02-18
Application Number : 90334
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BACLOFEN
Dosage Strength : 20MG
Approval Date : 2010-02-18
Application Number : 90334
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BACLOFEN
Dosage Strength : 5MG
Approval Date : 2025-01-31
Application Number : 90334
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMETANIDE
Dosage Strength : 0.5MG
Approval Date : 2024-09-18
Application Number : 212931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMETANIDE
Dosage Strength : 1MG
Approval Date : 2024-09-18
Application Number : 212931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMETANIDE
Dosage Strength : 2MG
Approval Date : 2024-09-18
Application Number : 212931
RX/OTC/DISCN : RX
RLD : No
TE Code : AB