Mirtazapine

Product NDC

61786-208

11-digit product format

617860208

Labeler code

61786

Product ID

61786-208_6b681794-ecfc-7986-e053-2991aa0a4fa9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mirtazapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077666

Marketing category

ANDA

Marketing start

2015-03-04

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