# Vestura

NDC: 0093-4000
Generic name: Drospirenone and Ethinyl Estradiol
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20210302
Marketing ended: 20260531
FDA application: ANDA078833

## 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:"0093-4000"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-4000
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ef288db4-abf9-4634-84e1-7925a81dcb67