up and up ibuprofen
- Product NDC
- 11673-314
- 11-digit product format
- 116730314
- Labeler code
- 11673
- Product ID
- 11673-314_7ffbb607-1dd7-432c-a747-f8474a154393
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2020-03-13
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-314 | UP AND UP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [TARGET CORPORATION] | 2 | Legacy NDC | 20200415_d6bb68ad-8cd2-4cab-b6af-4dd9bd2acb1f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-314-90 | 11673031490 | 500 TABLET, FILM COATED in 1 BOTTLE (11673-314-90) | 2020-03-13 | 0000-00-00 | No | No | Current |