# NORETHINDRONE

NDC: 0378-7292
Generic name: norethindrone
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130712

FDA application: ANDA201483

## Active ingredients

- NORETHINDRONE: .35 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-7292"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-7292
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af851d82-b30f-463b-9dba-0437225dc1ee