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Promethazine Hydrochloride - 55154-5112-5 - (Promethazine Hydrochloride)

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Drug Information of Promethazine Hydrochloride

Product NDC: 55154-5112
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: 55154-5112
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083312
Marketing Category: ANDA
Start Marketing Date: 19730919

Package Information of Promethazine Hydrochloride

Package NDC: 55154-5112-5
Package Description: 5 AMPULE in 1 BAG (55154-5112-5) > 1 mL in 1 AMPULE

NDC Information of Promethazine Hydrochloride

NDC Code 55154-5112-5
Proprietary Name Promethazine Hydrochloride
Package Description 5 AMPULE in 1 BAG (55154-5112-5) > 1 mL in 1 AMPULE
Product NDC 55154-5112
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19730919
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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