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Promethazine Hydrochloride - 65162-745-50 - (Promethazine Hydrochloride)

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Drug Information of Promethazine Hydrochloride

Product NDC: 65162-745
Proprietary Name: Promethazine Hydrochloride
Non Proprietary Name: Promethazine Hydrochloride
Active Ingredient(s): 12.5    mg/1 & nbsp;   Promethazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Promethazine Hydrochloride

Product NDC: 65162-745
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091179
Marketing Category: ANDA
Start Marketing Date: 20110303

Package Information of Promethazine Hydrochloride

Package NDC: 65162-745-50
Package Description: 500 TABLET in 1 BOTTLE (65162-745-50)

NDC Information of Promethazine Hydrochloride

NDC Code 65162-745-50
Proprietary Name Promethazine Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (65162-745-50)
Product NDC 65162-745
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110303
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine Hydrochloride


General Information