01 2ACETAZOLAMIDE
02 2AMINOCAPROIC ACID
03 2BACLOFEN
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 4LABETALOL HYDROCHLORIDE
14 2METRONIDAZOLE
15 2MODAFINIL
16 4PERPHENAZINE
17 3PRAZOSIN HYDROCHLORIDE
18 2RANITIDINE HYDROCHLORIDE
19 3SERTRALINE HYDROCHLORIDE
20 3SILDENAFIL CITRATE
21 1VALGANCICLOVIR HYDROCHLORIDE
22 2VENLAFAXINE HYDROCHLORIDE
01 10CAPSULE;ORAL
02 2FOR SOLUTION;ORAL
03 2TABLET, EXTENDED RELEASE;ORAL
04 42TABLET;ORAL
01 10.5MG
02 4100MG
03 210MG
04 1125MG
05 116MG
06 11GM
07 21MG
08 4200MG
09 120MG
10 2250MG
11 225MG
12 32MG
13 2300MG
14 2400MG
15 24MG
16 2500MG
17 350MG
18 150MG/ML
19 18MG
20 3EQ 100MG BASE
21 1EQ 10MG BASE
22 2EQ 150MG BASE
23 1EQ 1MG BASE
24 1EQ 225MG BASE
25 3EQ 25MG BASE
26 1EQ 2MG BASE
27 1EQ 300MG BASE
28 3EQ 50MG BASE
29 1EQ 5MG BASE
30 1EQ 75MG BASE
31 1EQ 75MG BASE/5ML
01 7DISCN
02 48RX
03 1Blank
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 : 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
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CHLORPROMAZINE HYDROCHLO...
Dosage Strength : 10MG
Approval Date : 2020-08-31
Application Number : 213590
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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