Mirtazapine

Product NDC

68071-4003

11-digit product format

680714003

Labeler code

68071

Product ID

68071-4003_544dd14b-ce39-2f1b-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mirtazapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA077666

Marketing category

ANDA

Marketing start

2007-08-22

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