# QUARTETTE
> **NDA204061** · New Drug Application · Sponsor: TEVA BRANDED PHARM · Approved 2013-03-28
## Drug
- **FDA Application Number:** NDA204061
- **Application type:** New Drug Application
- **Brand name:** QUARTETTE
- **Generic name:** LEVONORGESTREL/ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL
- **Active ingredients:** ETHINYL ESTRADIOL; LEVONORGESTREL
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** TEVA BRANDED PHARM
- **Manufacturer:** Teva Pharmaceuticals USA, Inc.
- **First approval:** 2013-03-28
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=204061)
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