Up and Up nicotine
- Product NDC
- 11673-532
- 11-digit product format
- 116730532
- Labeler code
- 11673
- Product ID
- 11673-532_133cfe85-329a-471a-9632-375c9ed5a29e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nicotine Polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA076779
- Marketing category
- ANDA
- Marketing start
- 2009-07-09
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 11673-532 | UP AND UP NICOTINE (NICOTINE POLACRILEX) GUM, CHEWING [TARGET CORPORATION] | 8 | Legacy NDC | 20210416_0f5777f7-0265-412e-8b8b-68672add2957.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-532-78 | 11673053278 | 100 BLISTER PACK in 1 CARTON (11673-532-78) > 1 GUM, CHEWING in 1 BLISTER PACK | 100 blister pack | 2009-07-09 | 0000-00-00 | No | No | Current |