Fluphenazine hydrochloride

Product NDC

70518-0457

11-digit product format

705180457

Labeler code

70518

Product ID

70518-0457_851b0856-5d6f-5d70-e053-2a91aa0a4e56

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Fluphenazine hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA089804

Marketing category

ANDA

Marketing start

2017-04-24

Marketing end

0000-00-00

Substance

FLUPHENAZINE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Phenothiazines [CS],Phenothiazine [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record