United States · FDA National Drug Code directory
Minocycline Hydrochloride
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
- 59651-337_2ef3b8ae-dd97-473f-bd81-c8c1b192c0ed
- Product NDC
- 59651-337
- Form
- TABLET, FILM COATED
- Composition / generic term
- Minocycline Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200501
- Source listing expiry
- 20261231
Source-listed ingredients
- MINOCYCLINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 CONTAINER (59651-337-01) · 59651-337-01
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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