# Norethindrone Acetate and Ethinyl Estradiol

NDC: 70700-101
Generic name: Norethindrone Acetate and Ethinyl Estradiol Tablets and Ferrous Fumarate Tablets
Labeler / Manufacturer: Xiromed, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: ORAL
Marketing started: 20180824

FDA application: ANDA209609

## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70700-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70700-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4bc4302-9484-465a-090d-47e1e0360b73