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Fluphenazine Hydrochloride - 0527-1791-05 - (Fluphenazine Hydrochloride)

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Drug Information of Fluphenazine Hydrochloride

Product NDC: 0527-1791
Proprietary Name: Fluphenazine Hydrochloride
Non Proprietary Name: Fluphenazine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Fluphenazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fluphenazine Hydrochloride

Product NDC: 0527-1791
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089743
Marketing Category: ANDA
Start Marketing Date: 20100927

Package Information of Fluphenazine Hydrochloride

Package NDC: 0527-1791-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-05)

NDC Information of Fluphenazine Hydrochloride

NDC Code 0527-1791-05
Proprietary Name Fluphenazine Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-05)
Product NDC 0527-1791
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluphenazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100927
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name FLUPHENAZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Fluphenazine Hydrochloride


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