# Levonorgestrel and Ethinyl Estradiol

NDC: 68462-637
Generic name: Levonorgestrel and Ethinyl Estradiol
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150409

FDA application: ANDA202791

## Active ingredients

- ETHINYL ESTRADIOL: 20 ug/1
- LEVONORGESTREL: 90 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-637"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-637
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44fbc5ae-5682-471f-a12a-955e8b4d233a