# Estradiol

NDC: 70954-564
Generic name: Estradiol
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230906

FDA application: ANDA217334

## Active ingredients

- ESTRADIOL: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-564"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-564
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3fe899db-a8cd-4a31-88fb-1129be96b4d9