Ibuprofen
- Product NDC
- 72189-643
- 11-digit product format
- 721890643
- Labeler code
- 72189
- Product ID
- 72189-643_4149108e-2a56-f78a-e063-6394a90a7c66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA078329
- Marketing category
- ANDA
- Marketing start
- 2025-09-30
- 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 | 197806 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-643-21 | Ibuprofen | 21 in 1 BOTTLE | TABLET, FILM COATED | 21 | | 3 |
| 72189-643-30 | Ibuprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
| 72189-643-60 | Ibuprofen | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-643-21 | 72189064321 | 21 TABLET, FILM COATED in 1 BOTTLE (72189-643-21) | 2025-09-30 | No | No | Current |
| 72189-643-30 | 72189064330 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-643-30) | 2025-09-30 | No | No | Current |
| 72189-643-60 | 72189064360 | 60 TABLET, FILM COATED in 1 BOTTLE (72189-643-60) | 2025-09-30 | No | No | Current |