# Norethindrone Acetate and Ethinyl Estradiol

NDC: 68462-132
Generic name: Norethindrone Acetate 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: 20160120

FDA application: ANDA206969

## Active ingredients

- ETHINYL ESTRADIOL: .02 mg/1
- NORETHINDRONE ACETATE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-132"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-132
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5a44f7a2-45f1-4d28-b9fb-61d9f2456422