United States · FDA National Drug Code directory
Loestrin 21 Day
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
- 51285-131_21f0dbf2-f0a8-447a-a975-482b4194b1eb
- Product NDC
- 51285-131
- Form
- TABLET
- Composition / generic term
- Norethindrone Acetate and Ethinyl Estradiol
- Labeler
- Teva Women's Health LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150226
- Source listing expiry
- 20261231
Source-listed ingredients
- NORETHINDRONE ACETATE — 1 mg/1
- ETHINYL ESTRADIOL — 20 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 POUCH in 1 CARTON (51285-131-97) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK · 51285-131-97
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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