Ibuwin Forte
- Product NDC
- 69729-157
- 11-digit product format
- 697290157
- Labeler code
- 69729
- Product ID
- 69729-157_0daf1b9c-b64c-5616-e063-6294a90ab3c2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- OPMX LLC
- Application
- ANDA079174
- Marketing category
- ANDA
- Marketing start
- 2023-12-29
- 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
- Ibuwin Forte
- 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 |
|---|
| 69729-157-10 | Ibuwin Forte | 10 in 1 BLISTER PACK | TABLET | 10 | | 1 |
| 69729-157-10 | Ibuwin Forte | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69729-157 | IBUWIN FORTE (IBUPROFEN) TABLET [OPMX LLC] | 1 | Current NDC, 2 package rows | 20231230_0daf1be9-ea38-461e-e063-6394a90a7954.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 |
|---|
| 69729-157-10 | 69729015710 | 1 BLISTER PACK in 1 CARTON (69729-157-10) / 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2023-12-29 | No | No | Current |