# LEVONORGESTREL AND ETHINYL ESTRADIOL

NDC: 0378-6550
Generic name: levonorgestrel and ethinyl estradiol
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20130816
Marketing ended: 20260630
FDA application: ANDA091663

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-6550"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-6550
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=27178b07-42bd-496d-aebb-d9428664ee72