United States · FDA National Drug Code directory
MINOXIDIL
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
- 53489-387_4a668fcd-612e-6944-e063-6394a90a9e2f
- Product NDC
- 53489-387
- Form
- TABLET
- Composition / generic term
- minoxidil
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19951214
- Source listing expiry
- 20271231
Source-listed ingredients
- MINOXIDIL — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (53489-387-01) · 53489-387-01
- 250 TABLET in 1 BOTTLE (53489-387-03) · 53489-387-03
- 500 TABLET in 1 BOTTLE (53489-387-05) · 53489-387-05
- 1000 TABLET in 1 BOTTLE (53489-387-10) · 53489-387-10
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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