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CYPROHEPTADINE HYDROCHLORIDE - 55154-3255-9 - (CYPROHEPTADINE HYDROCHLORIDE)

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Drug Information of CYPROHEPTADINE HYDROCHLORIDE

Product NDC: 55154-3255
Proprietary Name: CYPROHEPTADINE HYDROCHLORIDE
Non Proprietary Name: CYPROHEPTADINE HYDROCHLORIDE
Active Ingredient(s): 4    mg/1 & nbsp;   CYPROHEPTADINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CYPROHEPTADINE HYDROCHLORIDE

Product NDC: 55154-3255
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040644
Marketing Category: ANDA
Start Marketing Date: 20100615

Package Information of CYPROHEPTADINE HYDROCHLORIDE

Package NDC: 55154-3255-9
Package Description: 30 TABLET in 1 BLISTER PACK (55154-3255-9)

NDC Information of CYPROHEPTADINE HYDROCHLORIDE

NDC Code 55154-3255-9
Proprietary Name CYPROHEPTADINE HYDROCHLORIDE
Package Description 30 TABLET in 1 BLISTER PACK (55154-3255-9)
Product NDC 55154-3255
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CYPROHEPTADINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100615
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CYPROHEPTADINE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of CYPROHEPTADINE HYDROCHLORIDE


General Information