Home > National Drug Code (NDC) > Trifluoperazine Hydrochloride

Trifluoperazine Hydrochloride - 35356-823-60 - (trifluoperazine hydrochloride)

Alphabetical Index


Drug Information of Trifluoperazine Hydrochloride

Product NDC: 35356-823
Proprietary Name: Trifluoperazine Hydrochloride
Non Proprietary Name: trifluoperazine hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   trifluoperazine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Trifluoperazine Hydrochloride

Product NDC: 35356-823
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040209
Marketing Category: ANDA
Start Marketing Date: 20120822

Package Information of Trifluoperazine Hydrochloride

Package NDC: 35356-823-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-823-60)

NDC Information of Trifluoperazine Hydrochloride

NDC Code 35356-823-60
Proprietary Name Trifluoperazine Hydrochloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-823-60)
Product NDC 35356-823
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name trifluoperazine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120822
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name TRIFLUOPERAZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Trifluoperazine Hydrochloride


General Information