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Chlorpromazine Hydrochloride - 0781-5915-01 - (Chlorpromazine Hydrochloride)

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Drug Information of Chlorpromazine Hydrochloride

Product NDC: 0781-5915
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: 0781-5915
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084113
Marketing Category: ANDA
Start Marketing Date: 19740709

Package Information of Chlorpromazine Hydrochloride

Package NDC: 0781-5915-01
Package Description: 100 TABLET, SUGAR COATED in 1 BOTTLE (0781-5915-01)

NDC Information of Chlorpromazine Hydrochloride

NDC Code 0781-5915-01
Proprietary Name Chlorpromazine Hydrochloride
Package Description 100 TABLET, SUGAR COATED in 1 BOTTLE (0781-5915-01)
Product NDC 0781-5915
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlorpromazine Hydrochloride
Dosage Form Name TABLET, SUGAR COATED
Route Name ORAL
Start Marketing Date 19740709
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CHLORPROMAZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Chlorpromazine Hydrochloride


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