Ibuprofen
- Product NDC
- 69842-489
- 11-digit product format
- 698420489
- Labeler code
- 69842
- Product ID
- 69842-489_3ea99833-458e-904b-e063-6294a90adb55
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy.Inc.
- Application
- ANDA091237
- Marketing category
- ANDA
- Marketing start
- 2021-12-18
- 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 |
|---|
| 69842-489-34 | Ibuprofen | 225 in 1 BOTTLE | TABLET, COATED | 225 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-489 | IBUPROFEN TABLET, COATED [CVS PHARMACY.INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20230317_cd0c3404-9e9d-bfad-e053-2995a90a8719.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 |
|---|
| 69842-489-34 | 69842048934 | 225 TABLET, COATED in 1 BOTTLE (69842-489-34) | 2021-12-18 | 0000-00-00 | No | No | Current |