mirtazapine

Product NDC

43063-255

11-digit product format

430630255

Labeler code

43063

Product ID

43063-255_7d3b5445-9eaf-c912-e053-2991aa0a32ac

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

mirtazapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA076219

Marketing category

ANDA

Marketing start

2003-06-19

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