mirtazapine

Product NDC

0185-0222

11-digit product format

001850222

Labeler code

0185

Product ID

0185-0222_d423d909-f428-4514-9814-e0a6b94de27a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

mirtazapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Eon Labs, Inc.

Application

ANDA076219

Marketing category

ANDA

Marketing start

2003-06-19

Marketing end

0000-00-00

Substance

MIRTAZAPINE

Active strength

45 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record