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
- 0378-7292_952f8023-4a5f-746d-c678-388b50e8909c
- Product NDC
- 0378-7292
- Form
- TABLET
- Composition / generic term
- norethindrone
- Labeler
- Mylan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130712
- Source listing expiry
- 20261231
Source-listed ingredients
- NORETHINDRONE — .35 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 POUCH in 1 CARTON (0378-7292-53) / 1 BLISTER PACK in 1 POUCH (0378-7292-85) / 28 TABLET in 1 BLISTER PACK · 0378-7292-53
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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