# Drospirenone and Ethinyl Estradiol

NDC: 31722-945
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: 20200124

FDA application: ANDA213034

## 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:"31722-945"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-945
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a1f6ea0e-7c14-47c4-83a2-3797bd012eb4