Childrens Ibuprofen
- Product NDC
- 72162-2286
- 11-digit product format
- 721622286
- Labeler code
- 72162
- Product ID
- 72162-2286_779b9aed-8ec9-4779-a686-58cf9ef8848f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074937
- Marketing category
- ANDA
- Marketing start
- 2014-04-09
- Substance
- IBUPROFEN
- Active strength
- 100 mg/5mL
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 72162-2286-2 | 72162228602 | 1 BOTTLE in 1 CARTON (72162-2286-2) / 118 mL in 1 BOTTLE | 1 bottle | 2024-04-30 | No | No | Historical |