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TRIFLUOPERAZINE - 16590-305-30 - (TRIFLUOPERAZINE)

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Drug Information of TRIFLUOPERAZINE

Product NDC: 16590-305
Proprietary Name: TRIFLUOPERAZINE
Non Proprietary Name: TRIFLUOPERAZINE
Active Ingredient(s): 2    mg/1 & nbsp;   TRIFLUOPERAZINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TRIFLUOPERAZINE

Product NDC: 16590-305
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085786
Marketing Category: ANDA
Start Marketing Date: 19811120

Package Information of TRIFLUOPERAZINE

Package NDC: 16590-305-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16590-305-30)

NDC Information of TRIFLUOPERAZINE

NDC Code 16590-305-30
Proprietary Name TRIFLUOPERAZINE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16590-305-30)
Product NDC 16590-305
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRIFLUOPERAZINE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19811120
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name TRIFLUOPERAZINE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of TRIFLUOPERAZINE


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