Ibuprofen
- Product NDC
- 50090-2629
- 11-digit product format
- 500902629
- Labeler code
- 50090
- Product ID
- 50090-2629_f0c4785a-b0fb-439c-b323-1fa74881a338
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091625
- Marketing category
- ANDA
- Marketing start
- 2015-12-21
- Substance
- IBUPROFEN
- Active strength
- 600 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 | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 197805, 197806, 197807 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2629-0 | Ibuprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 55 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2629 | IBUPROFEN TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 55 | Current NDC, Legacy NDC, 1 package rows | 20250510_51de1183-d226-4869-a00a-f6c74e126a39.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2629-0 | 50090262900 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2629-0) | 2016-11-17 | 0000-00-00 | No | No | Current |