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Promethazine Hydrochloride - 43063-447-04 - (Promethazine Hydrochloride)

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Drug Information of Promethazine Hydrochloride

Product NDC: 43063-447
Proprietary Name: Promethazine Hydrochloride
Non Proprietary Name: Promethazine Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Promethazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Promethazine Hydrochloride

Product NDC: 43063-447
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091179
Marketing Category: ANDA
Start Marketing Date: 20110303

Package Information of Promethazine Hydrochloride

Package NDC: 43063-447-04
Package Description: 4 TABLET in 1 BOTTLE, PLASTIC (43063-447-04)

NDC Information of Promethazine Hydrochloride

NDC Code 43063-447-04
Proprietary Name Promethazine Hydrochloride
Package Description 4 TABLET in 1 BOTTLE, PLASTIC (43063-447-04)
Product NDC 43063-447
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Promethazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110303
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Promethazine Hydrochloride


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