Home > National Drug Code (NDC) > Promethazine Hydrochloride

Promethazine Hydrochloride - 52125-639-08 - (Promethazine Hydrochloride)

Alphabetical Index


Drug Information of Promethazine Hydrochloride

Product NDC: 52125-639
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: 52125-639
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083426
Marketing Category: ANDA
Start Marketing Date: 20130530

Package Information of Promethazine Hydrochloride

Package NDC: 52125-639-08
Package Description: 10 TABLET in 1 VIAL (52125-639-08)

NDC Information of Promethazine Hydrochloride

NDC Code 52125-639-08
Proprietary Name Promethazine Hydrochloride
Package Description 10 TABLET in 1 VIAL (52125-639-08)
Product NDC 52125-639
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130530
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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