Ibuprofen
- Product NDC
- 76420-847
- 11-digit product format
- 764200847
- Labeler code
- 76420
- Product ID
- 76420-847_2195e546-9f39-0130-e063-6294a90ad9c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA202413
- Marketing category
- ANDA
- Marketing start
- 2024-05-23
- Substance
- IBUPROFEN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WK2XYI10QM | IBUPROFEN | 15687-27-1 | IBUPROFEN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-847-01 | 76420084701 | 100 TABLET, FILM COATED in 1 BOTTLE (76420-847-01) | 2024-09-08 | No | No | Historical |
| 76420-847-05 | 76420084705 | 500 TABLET, FILM COATED in 1 BOTTLE (76420-847-05) | 2024-09-08 | No | No | Historical |
| 76420-847-30 | 76420084730 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-847-30) | 2024-09-08 | No | No | Historical |
| 76420-847-60 | 76420084760 | 60 TABLET, FILM COATED in 1 BOTTLE (76420-847-60) | 2024-09-08 | No | No | Historical |
| 76420-847-90 | 76420084790 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-847-90) | 2024-09-08 | No | No | Historical |