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CHLORPROMAZINE HYDROCHLORIDE - 24236-323-20 - (CHLORPROMAZINE HYDROCHLORIDE)

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Drug Information of CHLORPROMAZINE HYDROCHLORIDE

Product NDC: 24236-323
Proprietary Name: CHLORPROMAZINE HYDROCHLORIDE
Non Proprietary Name: CHLORPROMAZINE HYDROCHLORIDE
Active Ingredient(s): 25    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: 24236-323
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084112
Marketing Category: ANDA
Start Marketing Date: 20101216

Package Information of CHLORPROMAZINE HYDROCHLORIDE

Package NDC: 24236-323-20
Package Description: 100 TABLET, SUGAR COATED in 1 CANISTER (24236-323-20)

NDC Information of CHLORPROMAZINE HYDROCHLORIDE

NDC Code 24236-323-20
Proprietary Name CHLORPROMAZINE HYDROCHLORIDE
Package Description 100 TABLET, SUGAR COATED in 1 CANISTER (24236-323-20)
Product NDC 24236-323
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CHLORPROMAZINE HYDROCHLORIDE
Dosage Form Name TABLET, SUGAR COATED
Route Name ORAL
Start Marketing Date 20101216
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CHLORPROMAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of CHLORPROMAZINE HYDROCHLORIDE


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