Fluphenazine Hydrochloride

Product NDC

70518-2583

11-digit product format

705182583

Labeler code

70518

Product ID

70518-2583_b32484fd-784c-e6a0-e053-2995a90a77ba

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluphenazine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA089743

Marketing category

ANDA

Marketing start

2020-02-17

Marketing end

0000-00-00

Substance

FLUPHENAZINE HYDROCHLORIDE

Active strength

3 mg/1

Pharmacologic classes

Phenothiazines [CS],Phenothiazine [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record