# JUNEL FE 1/20
> **ANDA076081** · Abbreviated New Drug Application (Generic) · Sponsor: BARR · Approved 2003-09-18
## Drug
- **FDA Application Number:** ANDA076081
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** JUNEL FE 1/20
- **Generic name:** NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE
- **Active ingredients:** ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
- **Dosage form:** TABLET
- **Route:** ORAL-28
- **Marketing status:** Prescription
- **Sponsor:** BARR
- **Manufacturer:** Teva Pharmaceuticals USA, Inc.
- **First approval:** 2003-09-18
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=076081)
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