Loxapine

Product NDC

51079-902

11-digit product format

510790902

Labeler code

51079

Product ID

51079-902_97191904-b5d3-63b4-e053-2a95a90ae05e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

loxapine

Dosage form

CAPSULE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076762

Marketing category

ANDA

Marketing start

2004-12-15

Marketing end

2019-11-30

Substance

LOXAPINE SUCCINATE

Active strength

25 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record