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LOESTRIN 21 1/20

NDA · New Drug Application · Sponsor: TEVA BRANDED PHARM · Approved 1976-10-01

Drug application

FDA Application #

NDA017876

Application type

New Drug Application

Brand name

LOESTRIN 21 1/20

Generic name

Ethinyl Estradiol

Active ingredients

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Dosage form

TABLET

Route

ORAL-21

Marketing status

Discontinued

Sponsor

TEVA BRANDED PHARM

First approval

1976-10-01

Source

Authoritative

Drugs@FDA application overview

Machine

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