Ibuprofen
- Product NDC
- 71205-213
- 11-digit product format
- 712050213
- Labeler code
- 71205
- Product ID
- 71205-213_caf36ae7-7d2e-4058-aa5b-35122c1187ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA209207
- Marketing category
- ANDA
- Marketing start
- 2017-06-27
- 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
- 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 |
|---|
| 71205-213-72 | Ibuprofen | 120 mL in 1 BOTTLE | SUSPENSION | 120 | | 3 |
| 71205-213-72 | Ibuprofen | 1 in 1 CARTON | SUSPENSION | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-213 | IBUPROFEN SUSPENSION [PROFICIENT RX LP] | 3 | Current NDC, Legacy NDC, 2 package rows | 20220710_b7565aac-a928-4116-b9af-cf636da4537c.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 |
|---|
| 71205-213-72 | 71205021372 | 1 BOTTLE in 1 CARTON (71205-213-72) / 120 mL in 1 BOTTLE | 1 bottle | 2019-01-01 | 0000-00-00 | No | No | Current |