Nabumetone
NDC 70954-785, Nabumetone, tablet, film coated, from ANI Pharmaceuticals, Inc..
- Product NDC
- 70954-785
- Status
- Listed
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA219118
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70954-785 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NABUMETONE750 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70954-785-10 | 70954078510 | 100 TABLET, FILM COATED in 1 BOTTLE (70954-785-10) |
| 70954-785-20 | 70954078520 | 500 TABLET, FILM COATED in 1 BOTTLE (70954-785-20) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e87289f4-d4f9-4510-aaa5-51f8f8167658NADAC price for package 70954078510
GET /v1/drugs/nadac/70954078510
Use it
Look up 70954-785 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70954-785 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70954-785. 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.