Eszopiclone
NDC 70518-4361, Eszopiclone, tablet, film coated, from REMEDYREPACK INC..
- Product NDC
- 70518-4361
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205504
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4361 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ESZOPICLONE2 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4361-0 | 70518436100 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4361-0) |
| 70518-4361-1 | 70518436101 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4361-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/52ab8ee9-a04d-4e27-b0f4-eb050f144715
Use it
Look up 70518-4361 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4361 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4361. 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.