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Promethazine hydrochloride - 54868-4021-0 - (Promethazine hydrochloride)

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Drug Information of Promethazine hydrochloride

Product NDC: 54868-4021
Proprietary Name: Promethazine hydrochloride
Non Proprietary Name: Promethazine hydrochloride
Active Ingredient(s): 25    mg/mL & nbsp;   Promethazine hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Promethazine hydrochloride

Product NDC: 54868-4021
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040737
Marketing Category: ANDA
Start Marketing Date: 20000229

Package Information of Promethazine hydrochloride

Package NDC: 54868-4021-0
Package Description: 25 AMPULE in 1 CARTON (54868-4021-0) > 1 mL in 1 AMPULE

NDC Information of Promethazine hydrochloride

NDC Code 54868-4021-0
Proprietary Name Promethazine hydrochloride
Package Description 25 AMPULE in 1 CARTON (54868-4021-0) > 1 mL in 1 AMPULE
Product NDC 54868-4021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000229
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine hydrochloride


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