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promethazine hydrochloride - 68788-9679-3 - (promethazine hydrochloride)

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Drug Information of promethazine hydrochloride

Product NDC: 68788-9679
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: 68788-9679
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040863
Marketing Category: ANDA
Start Marketing Date: 20130424

Package Information of promethazine hydrochloride

Package NDC: 68788-9679-3
Package Description: 30 TABLET in 1 BOTTLE (68788-9679-3)

NDC Information of promethazine hydrochloride

NDC Code 68788-9679-3
Proprietary Name promethazine hydrochloride
Package Description 30 TABLET in 1 BOTTLE (68788-9679-3)
Product NDC 68788-9679
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name promethazine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130424
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name PROMETHAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of promethazine hydrochloride


General Information