United States · FDA National Drug Code directory
Etonogestrel and Ethinyl Estradiol
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0093-7679_d0827dbf-9df5-4438-a0c2-92d7d593e71c
- Product NDC
- 0093-7679
- Form
- INSERT, EXTENDED RELEASE
- Composition / generic term
- Etonogestrel and Ethinyl Estradiol
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210119 / 20270731
Source-listed ingredients
- ETONOGESTREL — .12 mg/d
- ETHINYL ESTRADIOL — .015 mg/d
These values do not establish equivalence or a dose recommendation.
Packages
- 3 POUCH in 1 CARTON (0093-7679-02) / 21 d in 1 POUCH (0093-7679-01) · 0093-7679-02
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →