Ibuprofen
- Product NDC
- 42291-442
- 11-digit product format
- 422910442
- Labeler code
- 42291
- Product ID
- 42291-442_d57cc4c3-b774-5ff8-e053-2995a90afadd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA078329
- Marketing category
- ANDA
- Marketing start
- 2020-09-03
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 800 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42291-442-30 | Ibuprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42291-442 | IBUPROFEN TABLET, FILM COATED [AVKARE] | 1 | Legacy NDC, 1 package rows | 20210602_c3b988ee-eff3-4578-e053-2995a90a1fcb.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 |
|---|
| 42291-442-30 | 42291044230 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-442-30) | 2021-06-01 | 0000-00-00 | No | No | Current |
| 42291-442-90 | 42291044290 | 90 TABLET, FILM COATED in 1 BOTTLE (42291-442-90) | 2020-09-24 | 0000-00-00 | No | No | Current |
| 42291-442-95 | 42291044295 | 500 TABLET, FILM COATED in 1 BOTTLE (42291-442-95) | 2020-09-03 | 0000-00-00 | No | No | Current |