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01 2DIPHENHYDRAMINE HYDROCHLORIDE
02 1DOXYLAMINE SUCCINATE
03 3IBUPROFEN
04 1LOPERAMIDE HYDROCHLORIDE
05 1METRONIDAZOLE
06 1NAPROXEN SODIUM
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01 8LNK
02 1LNK INTL INC
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01 2CAPSULE;ORAL
02 7TABLET;ORAL
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01 1100MG
02 2200MG
03 1220MG
04 1250MG
05 225MG
06 12MG
07 150MG
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01 9USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : DIPHENHYDRAMINE HYDROCHLO...
Dosage Strength : 25MG
Packaging :
Approval Date : 1983-01-27
Application Number : 87977
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : DIPHENHYDRAMINE HYDROCHLO...
Dosage Strength : 50MG
Packaging :
Approval Date : 1983-01-27
Application Number : 87978
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : DOXYLAMINE SUCCINATE
Dosage Strength : 25MG
Packaging :
Approval Date : 2004-08-27
Application Number : 40564
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : IBUPROFEN
Dosage Strength : 200MG
Packaging :
Approval Date : 1999-03-01
Application Number : 75010
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : IBUPROFEN
Dosage Strength : 200MG
Packaging :
Approval Date : 1999-03-01
Application Number : 75139
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : IBUPROFEN
Dosage Strength : 100MG
Packaging :
Approval Date : 2004-06-17
Application Number : 76741
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LOPERAMIDE HYDROCHLORIDE
Dosage Strength : 2MG
Packaging :
Approval Date : 2003-06-10
Application Number : 76497
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : METRONIDAZOLE
Dosage Strength : 250MG
Packaging :
Approval Date : 1984-04-10
Application Number : 19029
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : NAPROXEN SODIUM
Dosage Strength : 220MG
Packaging :
Approval Date : 2017-01-23
Application Number : 204872
Regulatory Info : OTC
Registration Country : USA