IBUPROFEN
NDC 72189-266, IBUPROFEN, tablet, film coated, from DIRECT RX.
- Product NDC
- 72189-266
- Status
- Listed
- Labeler
- DIRECT RX
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090796
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72189-266 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- IBUPROFEN800 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72189-266-15 | 72189026615 | 15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15) |
| 72189-266-30 | 72189026630 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30) |
| 72189-266-40 | 72189026640 | 40 TABLET, FILM COATED in 1 BOTTLE (72189-266-40) |
| 72189-266-60 | 72189026660 | 60 TABLET, FILM COATED in 1 BOTTLE (72189-266-60) |
| 72189-266-71 | 72189026671 | 100 TABLET, FILM COATED in 1 BOTTLE (72189-266-71) |
| 72189-266-72 | 72189026672 | 120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72) |
| 72189-266-90 | 72189026690 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c3f30813-0848-6e8a-e053-2995a90a3dea
Use it
Look up 72189-266 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72189-266 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72189-266. 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.