IBUPROFEN
NDC 72288-080, Ibuprofen, tablet, film coated, from Amazon.com Services LLC.
- Product NDC
- 72288-080
- Status
- Listed
- Labeler
- Amazon.com Services LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA072096
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72288-080 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- IBUPROFEN200 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72288-080-09 | 72288008009 | 50 POUCH in 1 CARTON (72288-080-09) / 2 TABLET, FILM COATED in 1 POUCH (72288-080-54) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 72288-080 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72288-080 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72288-080. 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.