Ibuprofen
- Product NDC
- 51672-2138
- 11-digit product format
- 516722138
- Labeler code
- 51672
- Product ID
- 51672-2138_82e13eb7-a786-4727-9f5d-956095aabad6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA209207
- Marketing category
- ANDA
- Marketing start
- 2018-09-12
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 100 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 51672-2138-1 | 51672213801 | 1 BOTTLE in 1 CARTON (51672-2138-1) > 240 mL in 1 BOTTLE | 1 bottle | 2018-09-12 | 0000-00-00 | No | No | Current |
| 51672-2138-8 | 51672213808 | 1 BOTTLE in 1 CARTON (51672-2138-8) > 120 mL in 1 BOTTLE | 1 bottle | 2018-09-12 | 0000-00-00 | No | No | Current |