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PROMETHAZINE HYDROCHLORIDE - 60429-151-01 - (PROMETHAZINE HYDROCHLORIDE)

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Drug Information of PROMETHAZINE HYDROCHLORIDE

Product NDC: 60429-151
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: 60429-151
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040713
Marketing Category: ANDA
Start Marketing Date: 20060731

Package Information of PROMETHAZINE HYDROCHLORIDE

Package NDC: 60429-151-01
Package Description: 100 TABLET in 1 BOTTLE (60429-151-01)

NDC Information of PROMETHAZINE HYDROCHLORIDE

NDC Code 60429-151-01
Proprietary Name PROMETHAZINE HYDROCHLORIDE
Package Description 100 TABLET in 1 BOTTLE (60429-151-01)
Product NDC 60429-151
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PROMETHAZINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060731
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, 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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