01 1ALBENDAZOLE
02 3BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
03 1CARBIDOPA
04 1COLESTIPOL HYDROCHLORIDE
05 4DILTIAZEM HYDROCHLORIDE
06 2GLYCOPYRROLATE
07 1IVERMECTIN
08 1LOPERAMIDE HYDROCHLORIDE
09 1MIGLUSTAT
10 4PREDNISOLONE SODIUM PHOSPHATE
11 2TINIDAZOLE
01 2CAPSULE;ORAL
02 4SOLUTION;ORAL
03 2TABLET, ORALLY DISINTEGRATING;ORAL
04 13TABLET;ORAL
01 10.85MG
02 11.7MG
03 1100MG
04 110MG;6.25MG
05 1120MG
06 11GM
07 12.5MG;6.25MG
08 1200MG
09 1250MG
10 125MG
11 12MG
12 130MG
13 13MG
14 1500MG
15 15MG;6.25MG
16 160MG
17 190MG
18 1EQ 10MG BASE/5ML
19 1EQ 15MG BASE/5ML
20 1EQ 20MG BASE/5ML
21 1EQ 25MG BASE/5ML
01 6DISCN
02 15RX
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ALBENDAZOLE
Dosage Strength : 200MG
Approval Date : 2019-05-14
Application Number : 211117
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : BISOPROLOL FUMARATE AND ...
Dosage Strength : 2.5MG;6.25MG
Approval Date : 2020-07-09
Application Number : 212678
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : BISOPROLOL FUMARATE AND ...
Dosage Strength : 5MG;6.25MG
Approval Date : 2020-07-09
Application Number : 212678
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : BISOPROLOL FUMARATE AND ...
Dosage Strength : 10MG;6.25MG
Approval Date : 2020-07-09
Application Number : 212678
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : CARBIDOPA
Dosage Strength : 25MG
Approval Date : 2016-02-17
Application Number : 205304
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : COLESTIPOL HYDROCHLORIDE
Dosage Strength : 1GM
Approval Date : 2024-08-16
Application Number : 217667
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DILTIAZEM HYDROCHLORIDE
Dosage Strength : 30MG
Approval Date : 2019-11-18
Application Number : 211596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DILTIAZEM HYDROCHLORIDE
Dosage Strength : 60MG
Approval Date : 2019-11-18
Application Number : 211596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DILTIAZEM HYDROCHLORIDE
Dosage Strength : 90MG
Approval Date : 2019-11-18
Application Number : 211596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DILTIAZEM HYDROCHLORIDE
Dosage Strength : 120MG
Approval Date : 2019-11-18
Application Number : 211596
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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