United States · FDA National Drug Code directory
Ramelteon
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
- 87063-189_51354e62-ab19-97a2-e063-6294a90ab08b
- Product NDC
- 87063-189
- Form
- TABLET
- Composition / generic term
- Ramelteon
- Labeler
- ASCLEMED USA INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230501
- Source listing expiry
- 20271231
Source-listed ingredients
- RAMELTEON — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (87063-189-01) · 87063-189-01
- 5 TABLET in 1 BOTTLE (87063-189-05) · 87063-189-05
- 10 TABLET in 1 BOTTLE (87063-189-10) · 87063-189-10
- 20 TABLET in 1 BOTTLE (87063-189-20) · 87063-189-20
- 30 TABLET in 1 BOTTLE (87063-189-30) · 87063-189-30
- 60 TABLET in 1 BOTTLE (87063-189-60) · 87063-189-60
- 90 TABLET in 1 BOTTLE (87063-189-90) · 87063-189-90
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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