CHILDRENS IBUPROFEN
- Product NDC
- 10202-711
- 11-digit product format
- 102020711
- Labeler code
- 10202
- Product ID
- 10202-711_08d0fef0-e393-4e8e-8193-3e6512814731
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- 7-Eleven
- Application
- ANDA209179
- Marketing category
- ANDA
- Marketing start
- 2019-05-06
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CHILDRENS IBUPROFEN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 100 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 197803 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10202-711-24 | CHILDRENS IBUPROFEN | 120 mL in 1 BOTTLE | SUSPENSION | 120 | | 5 |
| 10202-711-24 | CHILDRENS IBUPROFEN | 1 in 1 CARTON | SUSPENSION | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10202-711 | CHILDRENS IBUPROFEN (IBUPROFEN) SUSPENSION [7-ELEVEN] | 4 | Current NDC, Legacy NDC, 2 package rows | 20221105_af0ec23c-cefc-40a9-ab9a-03b8528d4e13.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10202-711-24 | 10202071124 | 1 BOTTLE in 1 CARTON (10202-711-24) / 120 mL in 1 BOTTLE | 1 bottle | 2019-05-06 | 0000-00-00 | No | No | Current |