PREGABALIN
NDC 72205-077, PREGABALIN, tablet, film coated, extended release, from Novadoz Pharmaceuticals LLC.
- Product NDC
- 72205-077
- Status
- Listed
- Labeler
- Novadoz Pharmaceuticals LLC
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213226
- DEA schedule
- CV
curl https://api.healthcare.dev/v1/drugs/ndc/72205-077 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREGABALIN82.5 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72205-077-30 | 72205007730 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-077-30) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f6aa5977-97c8-4a56-8e35-d9ab5cc24369NADAC price for package 72205007730
GET /v1/drugs/nadac/72205007730
Use it
Look up 72205-077 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72205-077 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72205-077. 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.