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Fluphenazine Hydrochloride - 49349-369-02 - (Fluphenazine Hydrochloride)

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Drug Information of Fluphenazine Hydrochloride

Product NDC: 49349-369
Proprietary Name: Fluphenazine Hydrochloride
Non Proprietary Name: Fluphenazine Hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   Fluphenazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Fluphenazine Hydrochloride

Product NDC: 49349-369
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089583
Marketing Category: ANDA
Start Marketing Date: 20110711

Package Information of Fluphenazine Hydrochloride

Package NDC: 49349-369-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-369-02)

NDC Information of Fluphenazine Hydrochloride

NDC Code 49349-369-02
Proprietary Name Fluphenazine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-369-02)
Product NDC 49349-369
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluphenazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110711
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name FLUPHENAZINE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Fluphenazine Hydrochloride


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