Ibuprofen
NDC 72789-565, Ibuprofen, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 72789-565
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202413
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72789-565 \ -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 |
|---|---|---|
| 72789-565-10 | 72789056510 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-10) |
| 72789-565-15 | 72789056515 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-15) |
| 72789-565-21 | 72789056521 | 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-21) |
| 72789-565-30 | 72789056530 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-30) |
| 72789-565-40 | 72789056540 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-40) |
| 72789-565-60 | 72789056560 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-60) |
| 72789-565-82 | 72789056582 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-82) |
| 72789-565-86 | 72789056586 | 360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-86) |
| 72789-565-90 | 72789056590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-90) |
| 72789-565-93 | 72789056593 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-93) |
| 72789-565-94 | 72789056594 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-94) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3a38add6-a114-4e18-836c-3bfc727db231
Use it
Look up 72789-565 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72789-565 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72789-565. 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.