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Fluphenazine Hydrochloride - 0121-0653-04 - (Fluphenazine Hydrochloride)

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Drug Information of Fluphenazine Hydrochloride

Product NDC: 0121-0653
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): SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluphenazine Hydrochloride

Product NDC: 0121-0653
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074725
Marketing Category: ANDA
Start Marketing Date: 20100901

Package Information of Fluphenazine Hydrochloride

Package NDC: 0121-0653-04
Package Description: 120 mL in 1 BOTTLE, DROPPER (0121-0653-04)

NDC Information of Fluphenazine Hydrochloride

NDC Code 0121-0653-04
Proprietary Name Fluphenazine Hydrochloride
Package Description 120 mL in 1 BOTTLE, DROPPER (0121-0653-04)
Product NDC 0121-0653
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluphenazine Hydrochloride
Dosage Form Name SOLUTION, CONCENTRATE
Route Name ORAL
Start Marketing Date 20100901
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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