up and up ibuprofen
- Product NDC
- 11673-647
- 11-digit product format
- 116730647
- Labeler code
- 11673
- Product ID
- 11673-647_d6eefb76-853a-48d5-ab95-68be4524dedd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2009-05-28
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-647-62 | 11673064762 | 1 BOTTLE in 1 CARTON (11673-647-62) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2009-05-28 | 0000-00-00 | No | No | Current |
| 11673-647-82 | 11673064782 | 1 BOTTLE in 1 CARTON (11673-647-82) > 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-02-23 | 0000-00-00 | No | No | Current |
| 11673-647-85 | 11673064785 | 1 BOTTLE in 1 CARTON (11673-647-85) > 250 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2009-06-12 | 0000-00-00 | No | No | Current |