Trifluoperazine Hydrochloride

Product NDC

0781-1036

11-digit product format

007811036

Labeler code

0781

Product ID

0781-1036_5a97a496-6669-4b98-a2e8-e87b8c7d556a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Trifluoperazine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA085788

Marketing category

ANDA

Marketing start

1981-11-20

Marketing end

0000-00-00

Substance

TRIFLUOPERAZINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Phenothiazine [EPC],Phenothiazines [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record