Loestrin

Product NDC

51285-129

11-digit product format

512850129

Labeler code

51285

Product ID

51285-129_966ca14a-7af3-40d1-9859-466784a6fd81

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate

Dosage form

KIT

Labeler

Teva Women's Health, Inc.

Application

ANDA076064

Marketing category

ANDA

Marketing start

2015-07-29

Marketing end

0000-00-00

Active strength

0

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record