up and up ibuprofen
- Product NDC
- 11673-183
- 11-digit product format
- 116730183
- Labeler code
- 11673
- Product ID
- 11673-183_9a5ec1c1-4590-458c-8777-ab8bc16c53fd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA077349
- Marketing category
- ANDA
- Marketing start
- 2010-03-11
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-183-83 | 11673018383 | 225 TABLET, FILM COATED in 1 BOTTLE (11673-183-83) | 2010-03-11 | 0000-00-00 | No | No | Current |