Mirtazapine

Product NDC

68071-1659

11-digit product format

680711659

Labeler code

68071

Product ID

68071-1659_549bf887-1ef0-6a75-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mirtazapine

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA076541

Marketing category

ANDA

Marketing start

2004-04-22

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