Ibuprofen
- Product NDC
- 79903-415
- 11-digit product format
- 799030415
- Labeler code
- 79903
- Product ID
- 79903-415_025f3636-fa4f-4669-8011-e95c9de615f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- WALMART INC.
- Application
- ANDA075139
- Marketing category
- ANDA
- Marketing start
- 2026-03-26
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ibuprofen
- Brand name suffix
- Dye Free
- Listing expiration
- 2027-12-31
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 |
|---|
| 79903-415-99 | IbuprofenDye Free | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 79903-415-99 | 79903041599 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-415-99) | 2026-03-26 | No | No | Current |