# Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium

NDC: 0781-4103
Generic name: Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20150801

FDA application: NDA022574

## 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:"0781-4103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-4103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6928f186-190d-4c40-beab-81cf80cd45cb