Ibuprofen
- Product NDC
- 63868-724
- 11-digit product format
- 638680724
- Labeler code
- 63868
- Product ID
- 63868-724_560679f3-86ef-4332-90a3-b2d92667ac53
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- ANDA074916
- Marketing category
- ANDA
- Marketing start
- 2020-03-09
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 100 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-724-04 | 63868072404 | 1 BOTTLE in 1 CARTON (63868-724-04) > 118 mL in 1 BOTTLE | 1 bottle | 2020-03-09 | 0000-00-00 | No | No | Current |