Mirtazapine

Product NDC

63739-356

11-digit product format

637390356

Labeler code

63739

Product ID

63739-356_4b4f22c0-a361-41c6-a9ed-02793189ac23

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mirtazapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA076119

Marketing category

ANDA

Marketing start

2007-09-14

Marketing end

0000-00-00

Substance

MIRTAZAPINE

Active strength

30 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record