Uline Ibuprofen
- Product NDC
- 69790-709
- 11-digit product format
- 697900709
- Labeler code
- 69790
- Product ID
- 69790-709_3e5d77e9-9142-41d7-e063-6294a90a365e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Uline
- Application
- ANDA079174
- Marketing category
- ANDA
- Marketing start
- 2022-04-04
- Substance
- IBUPROFEN
- Active strength
- 200 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Uline Ibuprofen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 310965 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69790-709-33 | Uline Ibuprofen | 50 in 1 BOX | TABLET | 50 | | 4 |
| 69790-709-33 | Uline Ibuprofen | 2 in 1 PACKET | TABLET | 2 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69790-709 | ULINE IBUPROFEN (IBUPROFEN) TABLET ULINE IBUPROFEN (IBUPROFEN) TABLET, COATED [ULINE] | 3 | Current NDC, Legacy NDC, 2 package rows | 20240129_d7342a15-9d49-74ed-e053-2a95a90a22cc.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 |
|---|
| 69790-709-33 | 69790070933 | 50 PACKET in 1 BOX (69790-709-33) / 2 TABLET in 1 PACKET | 50 packet | 2022-04-04 | 0000-00-00 | No | No | Current |