Home > National Drug Code (NDC) > Chlorpromazine Hydrochloride

Chlorpromazine Hydrochloride - 52125-062-02 - (Chlorpromazine Hydrochloride)

Alphabetical Index


Drug Information of Chlorpromazine Hydrochloride

Product NDC: 52125-062
Proprietary Name: Chlorpromazine Hydrochloride
Non Proprietary Name: Chlorpromazine Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Chlorpromazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, SUGAR COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Chlorpromazine Hydrochloride

Product NDC: 52125-062
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083386
Marketing Category: ANDA
Start Marketing Date: 20130221

Package Information of Chlorpromazine Hydrochloride

Package NDC: 52125-062-02
Package Description: 30 TABLET, SUGAR COATED in 1 BLISTER PACK (52125-062-02)

NDC Information of Chlorpromazine Hydrochloride

NDC Code 52125-062-02
Proprietary Name Chlorpromazine Hydrochloride
Package Description 30 TABLET, SUGAR COATED in 1 BLISTER PACK (52125-062-02)
Product NDC 52125-062
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlorpromazine Hydrochloride
Dosage Form Name TABLET, SUGAR COATED
Route Name ORAL
Start Marketing Date 20130221
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CHLORPROMAZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Chlorpromazine Hydrochloride


General Information