# LOESTRIN 21 1/20
> **NDA017876** · New Drug Application · Sponsor: TEVA BRANDED PHARM · Approved 1976-10-01
## Drug
- **FDA Application Number:** 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
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=017876)
---
*AI Analytics · CC0 1.0*