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promethazine hydrochloride - 0615-7668-05 - (promethazine hydrochloride)

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Drug Information of promethazine hydrochloride

Product NDC: 0615-7668
Proprietary Name: promethazine hydrochloride
Non Proprietary Name: promethazine hydrochloride
Active Ingredient(s): 25    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: 0615-7668
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040863
Marketing Category: ANDA
Start Marketing Date: 20090127

Package Information of promethazine hydrochloride

Package NDC: 0615-7668-05
Package Description: 15 TABLET in 1 BLISTER PACK (0615-7668-05)

NDC Information of promethazine hydrochloride

NDC Code 0615-7668-05
Proprietary Name promethazine hydrochloride
Package Description 15 TABLET in 1 BLISTER PACK (0615-7668-05)
Product NDC 0615-7668
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name promethazine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090127
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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