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Promethazine Hydrochloride - 54569-4168-0 - (Promethazine Hydrochloride)

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Drug Information of Promethazine Hydrochloride

Product NDC: 54569-4168
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: 54569-4168
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040712
Marketing Category: ANDA
Start Marketing Date: 20120717

Package Information of Promethazine Hydrochloride

Package NDC: 54569-4168-0
Package Description: 5 TABLET in 1 BOTTLE (54569-4168-0)

NDC Information of Promethazine Hydrochloride

NDC Code 54569-4168-0
Proprietary Name Promethazine Hydrochloride
Package Description 5 TABLET in 1 BOTTLE (54569-4168-0)
Product NDC 54569-4168
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 A-S Medication Solutions LLC
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