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Promethazine Hydrochloride - 21695-649-12 - (Promethazine Hydrochloride)

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Drug Information of Promethazine Hydrochloride

Product NDC: 21695-649
Proprietary Name: Promethazine Hydrochloride
Non Proprietary Name: Promethazine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Promethazine Hydrochloride
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of Promethazine Hydrochloride

Product NDC: 21695-649
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040500
Marketing Category: ANDA
Start Marketing Date: 20030630

Package Information of Promethazine Hydrochloride

Package NDC: 21695-649-12
Package Description: 1 BLISTER PACK in 1 CARTON (21695-649-12) > 12 SUPPOSITORY in 1 BLISTER PACK

NDC Information of Promethazine Hydrochloride

NDC Code 21695-649-12
Proprietary Name Promethazine Hydrochloride
Package Description 1 BLISTER PACK in 1 CARTON (21695-649-12) > 12 SUPPOSITORY in 1 BLISTER PACK
Product NDC 21695-649
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine Hydrochloride
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 20030630
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine Hydrochloride


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