Levonorgestrel and Ethinyl Estradiol and Ethinyl Estradiol

Product NDC

51862-489

11-digit product format

518620489

Labeler code

51862

Product ID

51862-489_1195bc39-7a36-4550-8e6e-2bc41d8e379f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Levonorgestrel and Ethinyl Estradiol and Ethinyl Estradiol

Dosage form

KIT

Labeler

Mayne Pharma Inc.

Application

NDA204061

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2018-03-26

Marketing end

0000-00-00

Active strength

0

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record