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Chlorpromazine Hydrochloride - 0781-1719-13 - (Chlorpromazine Hydrochloride)

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Drug Information of Chlorpromazine Hydrochloride

Product NDC: 0781-1719
Proprietary Name: Chlorpromazine Hydrochloride
Non Proprietary Name: Chlorpromazine Hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   Chlorpromazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Chlorpromazine Hydrochloride

Product NDC: 0781-1719
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080439
Marketing Category: ANDA
Start Marketing Date: 19730103

Package Information of Chlorpromazine Hydrochloride

Package NDC: 0781-1719-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-1719-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Chlorpromazine Hydrochloride

NDC Code 0781-1719-13
Proprietary Name Chlorpromazine Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (0781-1719-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0781-1719
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlorpromazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19730103
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CHLORPROMAZINE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Chlorpromazine Hydrochloride


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