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
- 70710-1344_6bc89997-a72b-415e-93d9-442ce2579bca
- Product NDC
- 70710-1344
- Form
- TABLET
- Composition / generic term
- Ramelteon
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190723
- Source listing expiry
- 20261231
Source-listed ingredients
- RAMELTEON — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (70710-1344-1) · 70710-1344-1
- 30 TABLET in 1 BOTTLE (70710-1344-3) · 70710-1344-3
- 500 TABLET in 1 BOTTLE (70710-1344-5) · 70710-1344-5
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →