United States · FDA National Drug Code directory
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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
- 59651-136_b785dba5-f0b0-4f74-8845-e845432932c0
- Product NDC
- 59651-136
- Form
- TABLET
- Composition / generic term
- NORETHINDRONE
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230106
- Source listing expiry
- 20261231
Source-listed ingredients
- NORETHINDRONE — .35 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (59651-136-28) / 1 TABLET in 1 BLISTER PACK · 59651-136-28
- 3 POUCH in 1 CARTON (59651-136-88) / 1 TABLET in 1 POUCH · 59651-136-88
- 6 POUCH in 1 CARTON (59651-136-92) / 1 TABLET in 1 POUCH · 59651-136-92
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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