# Lutera

NDC: 51862-028
Generic name: levonorgestrel and ethinyl estradiol
Labeler / Manufacturer: Mayne Pharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20160803

FDA application: ANDA076625

## 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:"51862-028"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51862-028
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b91ad328-f2f4-4f7d-82d3-daaada95f509