# Norethindrone acetate

NDC: 50742-267
Generic name: norethindrone acetate
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190829

FDA application: ANDA206490

## Active ingredients

- NORETHINDRONE ACETATE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-267"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-267
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2f39b608-cc62-4ff0-a52a-bc3343275269