United States · FDA National Drug Code directory
Norethindrone Acetate 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
- 68462-656_bc4774d0-9902-4678-af65-69d6a70d9983
- Product NDC
- 68462-656
- Form
- TABLET
- Composition / generic term
- Norethindrone Acetate and Ethinyl Estradiol
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150402
- Source listing expiry
- 20271231
Source-listed ingredients
- NORETHINDRONE ACETATE — .5 mg/1
- ETHINYL ESTRADIOL — 2.5 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 POUCH in 1 CARTON (68462-656-29) / 1 BLISTER PACK in 1 POUCH / 28 TABLET in 1 BLISTER PACK · 68462-656-29
- 90 TABLET in 1 BOTTLE (68462-656-90) · 68462-656-90
Source and coverage
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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.
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