Mirtazapine

Product NDC

70518-0102

11-digit product format

705180102

Labeler code

70518

Product ID

70518-0102_9f4b54ed-c425-4045-e053-2995a90aab1a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Mirtazapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076122

Marketing category

ANDA

Marketing start

2017-01-09

Marketing end

0000-00-00

Substance

MIRTAZAPINE

Active strength

30 mg/1

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record