Pregabalin
NDC 72888-049, Pregabalin, tablet, film coated, extended release, from Advagen Pharma Ltd..
- Product NDC
- 72888-049
- Status
- Listed
- Labeler
- Advagen Pharma Ltd.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215249
- DEA schedule
- CV
curl https://api.healthcare.dev/v1/drugs/ndc/72888-049 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PREGABALIN82.5 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72888-049-30 | 72888004930 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-049-30) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/2ffee7e7-bfa0-4933-9baf-7df55080816eNADAC price for package 72888004930
GET /v1/drugs/nadac/72888004930
Use it
Look up 72888-049 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72888-049 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72888-049. 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.