# Junel FE

NDC: 72189-215
Generic name: Junel FE
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211006

FDA application: ANDA076380

## Active ingredients

- ETHINYL ESTRADIOL: 20 ug/1
- NORETHINDRONE ACETATE: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-215"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-215
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ea62a66e-d45d-11be-e053-2a95a90a7801