Eszopiclone
NDC 68180-322, Eszopiclone, tablet, film coated, from Lupin Pharmaceuticals, Inc..
- Product NDC
- 68180-322
- Status
- Listed
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091124
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/68180-322 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ESZOPICLONE1 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68180-322-01 | 68180032201 | 100 TABLET, FILM COATED in 1 BOTTLE (68180-322-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7068c455-691e-4c56-9857-b7b4e13f4784
Use it
Look up 68180-322 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68180-322 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68180-322. 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.