IBU
- Product NDC
- 68071-3125
- 11-digit product format
- 680713125
- Labeler code
- 68071
- Product ID
- 68071-3125_d5930cc8-00b8-de99-e053-2a95a90ae51b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075682
- Marketing category
- ANDA
- Marketing start
- 2008-11-20
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3125-1 | 68071312501 | 21 TABLET in 1 BOTTLE (68071-3125-1) | 21 tablet | 2008-11-20 | 0000-00-00 | No | No | Current |
| 68071-3125-2 | 68071312502 | 20 TABLET in 1 BOTTLE (68071-3125-2) | 20 tablet | 2008-11-20 | 0000-00-00 | No | No | Current |
| 68071-3125-3 | 68071312503 | 30 TABLET in 1 BOTTLE (68071-3125-3) | 30 tablet | 2008-11-20 | 0000-00-00 | No | No | Current |
| 68071-3125-4 | 68071312504 | 40 TABLET in 1 BOTTLE (68071-3125-4) | 40 tablet | 2008-11-20 | 0000-00-00 | No | No | Current |
| 68071-3125-5 | 68071312505 | 50 TABLET in 1 BOTTLE (68071-3125-5) | 50 tablet | 2008-11-20 | 0000-00-00 | No | No | Current |
| 68071-3125-7 | 68071312507 | 15 TABLET in 1 BOTTLE (68071-3125-7) | 15 tablet | 2008-11-20 | 0000-00-00 | No | No | Current |
| 68071-3125-9 | 68071312509 | 90 TABLET in 1 BOTTLE (68071-3125-9) | 90 tablet | 2008-11-20 | 0000-00-00 | No | No | Current |