Ibuprofen
- Product NDC
- 11822-6159
- 11-digit product format
- 118226159
- Labeler code
- 11822
- Product ID
- 11822-6159_472fbf00-039e-4033-9aa3-dd93e87cfc84
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA074916
- Marketing category
- ANDA
- Marketing start
- 2021-12-03
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 100 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| WK2XYI10QM | IBUPROFEN | 15687-27-1 | IBUPROFEN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-6159-5 | 11822615905 | 1 BOTTLE in 1 CARTON (11822-6159-5) > 118 mL in 1 BOTTLE | 1 bottle | 2021-12-03 | 0000-00-00 | No | No | Current |