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Fluphenazine Hydrochloride - 0121-0654-02 - (Fluphenazine Hydrochloride)

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Drug Information of Fluphenazine Hydrochloride

Product NDC: 0121-0654
Proprietary Name: Fluphenazine Hydrochloride
Non Proprietary Name: Fluphenazine Hydrochloride
Active Ingredient(s): .5    mg/mL & nbsp;   Fluphenazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): ELIXIR
Coding System: National Drug Codes(NDC)

Labeler Information of Fluphenazine Hydrochloride

Product NDC: 0121-0654
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040106
Marketing Category: ANDA
Start Marketing Date: 20100831

Package Information of Fluphenazine Hydrochloride

Package NDC: 0121-0654-02
Package Description: 60 mL in 1 BOTTLE (0121-0654-02)

NDC Information of Fluphenazine Hydrochloride

NDC Code 0121-0654-02
Proprietary Name Fluphenazine Hydrochloride
Package Description 60 mL in 1 BOTTLE (0121-0654-02)
Product NDC 0121-0654
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluphenazine Hydrochloride
Dosage Form Name ELIXIR
Route Name ORAL
Start Marketing Date 20100831
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, Inc.
Substance Name FLUPHENAZINE HYDROCHLORIDE
Strength Number .5
Strength Unit mg/mL
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Fluphenazine Hydrochloride


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