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01 2CETIRIZINE HYDROCHLORIDE
02 2CIMETIDINE
03 4FAMOTIDINE
04 2FEXOFENADINE HYDROCHLORIDE
05 1FOLIC ACID
06 9IBUPROFEN
07 1IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
08 1LOPERAMIDE HYDROCHLORIDE
09 2NAPROXEN SODIUM
10 1PREDNISONE
11 1QUINIDINE SULFATE
12 1RANITIDINE HYDROCHLORIDE
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01 27CONTRACT PHARMACAL
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01 1CAPSULE;ORAL
02 26TABLET;ORAL
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01 210MG
02 1180MG
03 11MG
04 7200MG
05 1200MG;30MG
06 220MG
07 2220MG
08 12MG
09 2400MG
10 140MG
11 25MG
12 1600MG
13 160MG
14 2800MG
15 1EQ 75MG BASE
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01 27USA
Regulatory Info : OTC
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : CETIRIZINE HYDROCHLORIDE ...
Dosage Strength : 5MG
Packaging :
Approval Date : 2007-12-27
Application Number : 76047
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : CETIRIZINE HYDROCHLORIDE ...
Dosage Strength : 10MG
Packaging :
Approval Date : 2007-12-27
Application Number : 76047
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : CIMETIDINE
Dosage Strength : 200MG
Packaging :
Approval Date : 1998-06-19
Application Number : 74961
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : CIMETIDINE
Dosage Strength : 200MG
Packaging :
Approval Date : 1998-06-19
Application Number : 74963
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : FAMOTIDINE
Dosage Strength : 20MG
Packaging :
Approval Date : 2023-12-20
Application Number : 217669
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : FAMOTIDINE
Dosage Strength : 40MG
Packaging :
Approval Date : 2023-12-20
Application Number : 217669
Regulatory Info : RX
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : FAMOTIDINE
Dosage Strength : 10MG
Packaging :
Approval Date : 2024-05-28
Application Number : 218003
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : FAMOTIDINE
Dosage Strength : 20MG
Packaging :
Approval Date : 2024-05-28
Application Number : 218003
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : FEXOFENADINE HYDROCHLORID...
Dosage Strength : 60MG
Packaging :
Approval Date : 2025-02-28
Application Number : 219032
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Contract Pharmacal Corporation
Dosage Form : TABLET;ORAL
Brand Name : FEXOFENADINE HYDROCHLORID...
Dosage Strength : 180MG
Packaging :
Approval Date : 2025-02-28
Application Number : 219032
Regulatory Info : OTC
Registration Country : USA