Ibuprofen
NDC 54348-825, IBUPROFEN, tablet, film coated, from PharmPak, Inc..
- Product NDC
- 54348-825
- Status
- Listed
- Labeler
- PharmPak, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091625
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/54348-825 \ -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 |
|---|---|---|
| 54348-825-00 | 54348082500 | 1 BOTTLE in 1 BOX (54348-825-00) / 1 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-06 | 54348082506 | 1 BOTTLE in 1 BOX (54348-825-06) / 6 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-08 | 54348082508 | 1 BOTTLE in 1 BOX (54348-825-08) / 8 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-09 | 54348082509 | 1 BOTTLE in 1 BOX (54348-825-09) / 9 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-10 | 54348082510 | 1 BOTTLE in 1 BOX (54348-825-10) / 10 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-12 | 54348082512 | 1 BOTTLE in 1 BOX (54348-825-12) / 12 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-15 | 54348082515 | 1 BOTTLE in 1 BOX (54348-825-15) / 15 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-20 | 54348082520 | 1 BOTTLE in 1 BOX (54348-825-20) / 20 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-30 | 54348082530 | 1 BOTTLE in 1 BOX (54348-825-30) / 30 TABLET, FILM COATED in 1 BOTTLE |
| 54348-825-60 | 54348082560 | 1 BOTTLE in 1 BOX (54348-825-60) / 60 TABLET, FILM COATED in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b493bf76-1e8b-4e72-bef6-aca4efc69cbe
Use it
Look up 54348-825 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/54348-825 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 54348-825. 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.