IBUPROFEN
NDC 71335-1517, IBUPROFEN, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-1517
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- 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/71335-1517 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- IBUPROFEN400 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-1517-1 | 71335151701 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1) |
| 71335-1517-2 | 71335151702 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2) |
| 71335-1517-3 | 71335151703 | 40 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3) |
| 71335-1517-4 | 71335151704 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4) |
| 71335-1517-5 | 71335151705 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5) |
| 71335-1517-6 | 71335151706 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6) |
| 71335-1517-7 | 71335151707 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7) |
| 71335-1517-8 | 71335151708 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8) |
| 71335-1517-9 | 71335151709 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6d189e86-4c36-43f5-b406-a342458d4155
Use it
Look up 71335-1517 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1517 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-1517. 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.