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Promethazine Hydrochloride - 50436-4379-2 - (Promethazine Hydrochloride)

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Drug Information of Promethazine Hydrochloride

Product NDC: 50436-4379
Proprietary Name: Promethazine Hydrochloride
Non Proprietary Name: Promethazine Hydrochloride
Active Ingredient(s): 25    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: 50436-4379
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040712
Marketing Category: ANDA
Start Marketing Date: 20120717

Package Information of Promethazine Hydrochloride

Package NDC: 50436-4379-2
Package Description: 12 TABLET in 1 BOTTLE (50436-4379-2)

NDC Information of Promethazine Hydrochloride

NDC Code 50436-4379-2
Proprietary Name Promethazine Hydrochloride
Package Description 12 TABLET in 1 BOTTLE (50436-4379-2)
Product NDC 50436-4379
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120717
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine Hydrochloride


General Information