Aftera

Product NDC

51285-103

11-digit product format

512850103

Labeler code

51285

Product ID

51285-103_283cb508-22ab-45f4-aa58-c4b182a00a2f

Type

HUMAN OTC DRUG

Nonproprietary name

levonorgestrel

Dosage form

TABLET

Route

ORAL

Labeler

Teva Women's Health, Inc.

Application

NDA021998

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-10-20

Marketing end

2020-05-31

Substance

LEVONORGESTREL

Active strength

2 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record