Ibuprofen
- Product NDC
- 36800-292
- 11-digit product format
- 368000292
- Labeler code
- 36800
- Product ID
- 36800-292_2c7a2c8d-cf4e-432d-9fe0-870eaf5b9e75
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Topco Associates, LLC
- Application
- ANDA075010
- Marketing category
- ANDA
- Marketing start
- 1988-05-24
- 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 |
|---|
| 36800-292-06 | Ibuprofen | 200 in 1 BOTTLE | TABLET, FILM COATED | 200 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-292 | IBUPROFEN TABLET, FILM COATED [TOPCO ASSOCIATES, LLC] | 12 | Current NDC, Legacy NDC, 1 package rows | 20240606_59a88ca7-eb37-46de-9134-a5a6d330bd49.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 |
|---|
| 36800-292-06 | 36800029206 | 200 TABLET, FILM COATED in 1 BOTTLE (36800-292-06) | 1988-05-24 | 0000-00-00 | No | No | Current |