Ibuprofen
- Product NDC
- 30142-647
- 11-digit product format
- 301420647
- Labeler code
- 30142
- Product ID
- 30142-647_f8cb0ac4-b0f0-415b-bcf4-fcef3a3cab7b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 1990-10-15
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 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
- 2023-12-31
- 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 |
|---|
| 30142-647-62 | 30142064762 | 1 BOTTLE in 1 CARTON (30142-647-62) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2007-10-23 | 0000-00-00 | No | No | Current |
| 30142-647-76 | 30142064776 | 1 BOTTLE in 1 CARTON (30142-647-76) > 120 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2002-04-05 | 0000-00-00 | No | No | Current |
| 30142-647-78 | 30142064778 | 1 BOTTLE in 1 CARTON (30142-647-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1994-11-04 | 0000-00-00 | No | No | Current |
| 30142-647-90 | 30142064790 | 500 TABLET, FILM COATED in 1 BOTTLE (30142-647-90) | | 2004-05-10 | 0000-00-00 | No | No | Current |