# norelgestromin and ethinyl estradiol

NDC: 70710-1190
Generic name: norelgestromin and ethinyl estradiol
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: PATCH
Routes: TRANSDERMAL
Marketing started: 20231121

FDA application: ANDA214594

## Active ingredients

- ETHINYL ESTRADIOL: 35 ug/mg
- NORELGESTROMIN: 150 ug/mg

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=10fa1458-c8ed-4197-922a-1ba7271d2b02