ibuprofen
- Product NDC
- 55910-901
- 11-digit product format
- 559100901
- Labeler code
- 55910
- Product ID
- 55910-901_f0b3ed7d-1622-3990-e053-2995a90ae520
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- DOLGENCORP INC
- Application
- ANDA091239
- Marketing category
- ANDA
- Marketing start
- 2019-12-09
- 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 |
|---|
| 55910-901-42 | ibuprofen | 24 in 1 BOTTLE | TABLET, COATED | 24 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55910-901 | IBUPROFEN TABLET, COATED [DOLGENCORP INC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230103_8f1358aa-495a-23da-e053-2995a90aa430.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 |
|---|
| 55910-901-42 | 55910090142 | 24 TABLET, COATED in 1 BOTTLE (55910-901-42) | 2019-12-09 | 0000-00-00 | No | No | Current |