United States · FDA National Drug Code directory
NORETHINDRONE
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
- 68180-876_21d08d75-2957-4610-94c1-76c844ba2f1b
- Product NDC
- 68180-876
- Form
- TABLET
- Composition / generic term
- NORETHINDRONE
- Labeler
- Lupin Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201111
- Source listing expiry
- 20261231
Source-listed ingredients
- NORETHINDRONE — .35 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (68180-876-73) / 28 TABLET in 1 BLISTER PACK · 68180-876-73
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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