01 2CETIRIZINE HYDROCHLORIDE
02 2CIMETIDINE
03 4FAMOTIDINE
04 1FOLIC ACID
05 9IBUPROFEN
06 1IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
07 1LOPERAMIDE HYDROCHLORIDE
08 2NAPROXEN SODIUM
09 1PREDNISONE
10 1QUINIDINE SULFATE
11 1RANITIDINE HYDROCHLORIDE
01 1CAPSULE;ORAL
02 24TABLET;ORAL
01 210MG
02 11MG
03 7200MG
04 1200MG;30MG
05 220MG
06 2220MG
07 12MG
08 2400MG
09 140MG
10 25MG
11 1600MG
12 2800MG
13 1EQ 75MG BASE
01 13DISCN
02 5OTC
03 5RX
04 2Blank
RLD : No
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 5MG
Approval Date : 2007-12-27
Application Number : 76047
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : CETIRIZINE HYDROCHLORIDE...
Dosage Strength : 10MG
Approval Date : 2007-12-27
Application Number : 76047
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : CIMETIDINE
Dosage Strength : 200MG
Approval Date : 1998-06-19
Application Number : 74961
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : CIMETIDINE
Dosage Strength : 200MG
Approval Date : 1998-06-19
Application Number : 74963
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 20MG
Approval Date : 2023-12-20
Application Number : 217669
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 40MG
Approval Date : 2023-12-20
Application Number : 217669
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 10MG
Approval Date : 2024-05-28
Application Number : 218003
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : FAMOTIDINE
Dosage Strength : 20MG
Approval Date : 2024-05-28
Application Number : 218003
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : FOLIC ACID
Dosage Strength : 1MG
Approval Date : 1982-01-01
Application Number : 85061
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD :
TE Code :
Contract Pharmacal Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 400MG
Approval Date :
Application Number : 71267
RX/OTC/DISCN :
RLD :
TE Code :
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