# Drospirenone and ethinyl estradiol

NDC: 31722-934
Generic name: Drospirenone and ethinyl estradiol
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20190322

FDA application: ANDA211944

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-934"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-934
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=71f90c73-63c2-432b-b112-cbdbd26b965c