Loxapine

Product NDC

51079-903

11-digit product format

510790903

Labeler code

51079

Product ID

51079-903_7cd92e8c-b4e0-1c1f-e053-2a91aa0a13df

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

0000-00-00

Substance

LOXAPINE SUCCINATE

Active strength

50 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record