Fluphenazine Hydrochloride

Product NDC

0781-1439

11-digit product format

007811439

Labeler code

0781

Product ID

0781-1439_f404131c-0b3b-4615-a708-d28d56f9af81

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluphenazine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA089586

Marketing category

ANDA

Marketing start

1987-10-16

Marketing end

2019-10-31

Substance

FLUPHENAZINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Phenothiazines [CS],Phenothiazine [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record