Mirtazapine

Product NDC

50436-3897

11-digit product format

504363897

Labeler code

50436

Product ID

50436-3897_fdf14401-b3e3-4f14-a7da-351d7898be6e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mirtazapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA076312

Marketing category

ANDA

Marketing start

2003-06-19

Marketing end

0000-00-00

Substance

MIRTAZAPINE

Active strength

15 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record