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Promethazine hydrochloride - 0143-9868-22 - (Promethazine hydrochloride)

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Drug Information of Promethazine hydrochloride

Product NDC: 0143-9868
Proprietary Name: Promethazine hydrochloride
Non Proprietary Name: Promethazine hydrochloride
Active Ingredient(s): 50    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: 0143-9868
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040737
Marketing Category: ANDA
Start Marketing Date: 20080424

Package Information of Promethazine hydrochloride

Package NDC: 0143-9868-22
Package Description: 1 mL in 1 AMPULE (0143-9868-22)

NDC Information of Promethazine hydrochloride

NDC Code 0143-9868-22
Proprietary Name Promethazine hydrochloride
Package Description 1 mL in 1 AMPULE (0143-9868-22)
Product NDC 0143-9868
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080424
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine hydrochloride


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