Ramelteon
NDC 52817-235, Ramelteon, tablet, film coated, from TruPharma, LLC.
- Product NDC
- 52817-235
- Status
- Listed
- Labeler
- TruPharma, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212650
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/52817-235 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- RAMELTEON8 mg/1
Pharmacologic classes
Melatonin Receptor Agonist [EPC]; Melatonin Receptor Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 52817-235-10 | 52817023510 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52817-235-10) |
| 52817-235-30 | 52817023530 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52817-235-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3d0cc378-4bc5-425c-8f41-43eb734c24d9NADAC price for package 52817023510
GET /v1/drugs/nadac/52817023510NADAC price for package 52817023530
GET /v1/drugs/nadac/52817023530
Use it
Look up 52817-235 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/52817-235 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 52817-235. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.