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Chlorpromazine - 0615-1547-39 - (Chlorpromazine Hydrochloride)

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Drug Information of Chlorpromazine

Product NDC: 0615-1547
Proprietary Name: Chlorpromazine
Non Proprietary Name: Chlorpromazine Hydrochloride
Active Ingredient(s): 50    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

Product NDC: 0615-1547
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080439
Marketing Category: ANDA
Start Marketing Date: 19730103

Package Information of Chlorpromazine

Package NDC: 0615-1547-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-1547-39)

NDC Information of Chlorpromazine

NDC Code 0615-1547-39
Proprietary Name Chlorpromazine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-1547-39)
Product NDC 0615-1547
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 NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name CHLORPROMAZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Chlorpromazine


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