Chlorpromazine Hydrochloride

Product NDC

51079-519

11-digit product format

510790519

Labeler code

51079

Product ID

51079-519_9a252b62-8427-382e-e053-2995a90a3222

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Chlorpromazine Hydrochloride

Dosage form

TABLET, SUGAR COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA084112

Marketing category

ANDA

Marketing start

1994-11-23

Marketing end

2021-01-31

Substance

CHLORPROMAZINE HYDROCHLORIDE

Active strength

25 mg/1

Pharmacologic classes

Phenothiazines [CS],Phenothiazine [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record