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Chlorpromazine Hydrochloride - 24236-581-28 - (Chlorpromazine Hydrochloride)

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Drug Information of Chlorpromazine Hydrochloride

Product NDC: 24236-581
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
Coding System: National Drug Codes(NDC)

Labeler Information of Chlorpromazine Hydrochloride

Product NDC: 24236-581
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084113
Marketing Category: ANDA
Start Marketing Date: 20100804

Package Information of Chlorpromazine Hydrochloride

Package NDC: 24236-581-28
Package Description: 300 TABLET in 1 CANISTER (24236-581-28)

NDC Information of Chlorpromazine Hydrochloride

NDC Code 24236-581-28
Proprietary Name Chlorpromazine Hydrochloride
Package Description 300 TABLET in 1 CANISTER (24236-581-28)
Product NDC 24236-581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlorpromazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100804
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


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