Ibuprofen
- Product NDC
- 71862-007
- 11-digit product format
- 718620007
- Labeler code
- 71862
- Product ID
- 71862-007_c125b554-d015-7ff6-e053-2a95a90a67c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Landmark Supply Inc.
- Application
- ANDA202413
- Marketing category
- ANDA
- Marketing start
- 2017-12-01
- 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
- 2022-12-31
- 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 |
|---|
| 71862-007-01 | Ibuprofen | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71862-007 | IBUPROFEN TABLET [LANDMARK SUPPLY INC.] | 2 | Legacy NDC, 1 package rows | 20210501_f2eb2137-c45f-41c3-8619-a43db9a4116c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71862-007-01 | 71862000701 | 100 TABLET in 1 BOTTLE (71862-007-01) | 100 tablet | 2017-12-01 | 0000-00-00 | No | No | Current |