Prochlorperazine Maleate

Product NDC

71335-0633

11-digit product format

713350633

Labeler code

71335

Product ID

71335-0633_bae0cd4d-12c1-4bc7-9a80-7b42c6f51e6b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prochlorperazine Maleate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA040120

Marketing category

ANDA

Marketing start

1996-07-25

Marketing end

0000-00-00

Substance

PROCHLORPERAZINE MALEATE

Active strength

5 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