Ibuprofen
- Product NDC
- 82501-1582
- 11-digit product format
- 825011582
- Labeler code
- 82501
- Product ID
- 82501-1582_ee17d117-e438-f5a6-e053-2a95a90a918b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Gobrands, Inc
- Application
- ANDA079129
- Marketing category
- ANDA
- Marketing start
- 2022-07-05
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82501-1582-1 | Ibuprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82501-1582 | IBUPROFEN TABLET, FILM COATED [GOBRANDS, INC] | 5 | Legacy NDC, 1 package rows | 20241222_6a19751a-9689-4a53-9b61-32d52dd41f39.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 |
|---|
| 82501-1582-1 | 82501158201 | 100 TABLET, FILM COATED in 1 BOTTLE (82501-1582-1) | 2022-07-05 | 0000-00-00 | No | No | Current |