Prochlorperazine Maleate

Product NDC

70518-0768

11-digit product format

705180768

Labeler code

70518

Product ID

70518-0768_8e7e053b-537c-62f8-e053-2995a90a07f2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

prochlorperazine maleate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA040185

Marketing category

ANDA

Marketing start

2017-10-09

Marketing end

0000-00-00

Substance

PROCHLORPERAZINE MALEATE

Active strength

10 mg/1

Pharmacologic classes

Phenothiazine [EPC],Phenothiazines [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record