IBUPROFEN
- Product NDC
- 11822-7892
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- RITE AID CORPORATION
- Application
- ANDA091239
- Marketing category
- ANDA
- Substance
- IBUPROFEN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 11822-7892-0 | 24 TABLET, COATED in 1 BOTTLE (11822-7892-0) | 2020-06-01 | | No | Historical |
| 11822-7892-2 | 50 TABLET, COATED in 1 BOTTLE (11822-7892-2) | 2020-06-01 | | No | Historical |
| 11822-7892-5 | 100 TABLET, COATED in 1 BOTTLE (11822-7892-5) | 2020-06-01 | | No | Historical |
| 11822-7892-7 | 200 TABLET, COATED in 1 BOTTLE (11822-7892-7) | 2020-06-01 | | No | Historical |
| 11822-7892-9 | 500 TABLET, COATED in 1 BOTTLE (11822-7892-9) | 2020-06-01 | | No | Historical |