Ibuprofen Oral
- Product NDC
- 68788-7984
- 11-digit product format
- 687887984
- Labeler code
- 68788
- Product ID
- 68788-7984_02d2e57b-981a-4714-a6a0-916cc9b02b05
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen Oral
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA210602
- Marketing category
- ANDA
- Marketing start
- 2021-08-05
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 100 mg/5mL
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7984 | IBUPROFEN ORAL SUSPENSION [PREFERRED PHARMACEUTICALS INC.] | 5 | Legacy NDC | 20250228_8ccce5d5-a3fa-454f-b193-1222083b5680.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7984-1 | 68788798401 | 1 BOTTLE in 1 CARTON (68788-7984-1) > 118 mL in 1 BOTTLE | 1 bottle | 2021-08-05 | 0000-00-00 | No | No | Current |