# Etonogestrel and Ethinyl Estradiol

NDC: 0093-7679
Generic name: Etonogestrel and Ethinyl Estradiol
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INSERT, EXTENDED RELEASE
Routes: VAGINAL
Marketing started: 20210119
Marketing ended: 20270731
FDA application: ANDA204305

## Active ingredients

- ETHINYL ESTRADIOL: .015 mg/d
- ETONOGESTREL: .12 mg/d

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-7679"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7679
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8cc104a-d522-49ad-af54-2f312b829b61