Ibuprofen
- Product NDC
- 0363-9593
- 11-digit product format
- 003639593
- Labeler code
- 0363
- Product ID
- 0363-9593_46549a71-13b9-ea53-e063-6294a90aef35
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Walgreens
- Application
- ANDA202312
- Marketing category
- ANDA
- Marketing start
- 2024-05-01
- 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
- 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 |
|---|
| 0363-9593-21 | Ibuprofen | 225 in 1 BOTTLE | TABLET | 225 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-9593 | IBUPROFEN TABLET [WALGREENS] | 2 | Current NDC, 1 package rows | 20240501_07edb8d0-2fa8-4b40-e063-6294a90a2fe9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-9593-21 | 00363959321 | 225 TABLET in 1 BOTTLE (0363-9593-21) | 225 tablet | 2024-05-01 | No | No | Historical |