Loxapine

Product NDC

70518-0995

11-digit product format

705180995

Labeler code

70518

Product ID

70518-0995_8f839791-308e-2319-e053-2a95a90a0f7d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

loxapine

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076762

Marketing category

ANDA

Marketing start

2018-01-29

Marketing end

0000-00-00

Substance

LOXAPINE SUCCINATE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record