# Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate

NDC: 60219-1031
Generic name: Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20170921

FDA application: ANDA207514

## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60219-1031"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60219-1031
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4fa03d8-0ae0-497f-ba4e-76f03fd7a3ab