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Fluphenazine Hydrochloride - 51079-487-20 - (fluphenazine hydrochloride)

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Drug Information of Fluphenazine Hydrochloride

Product NDC: 51079-487
Proprietary Name: Fluphenazine Hydrochloride
Non Proprietary Name: fluphenazine hydrochloride
Active Ingredient(s): 5    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: 51079-487
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089804
Marketing Category: ANDA
Start Marketing Date: 20110715

Package Information of Fluphenazine Hydrochloride

Package NDC: 51079-487-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-487-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-487-01)

NDC Information of Fluphenazine Hydrochloride

NDC Code 51079-487-20
Proprietary Name Fluphenazine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-487-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-487-01)
Product NDC 51079-487
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluphenazine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110715
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name FLUPHENAZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Complete Information of Fluphenazine Hydrochloride


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