Up and Up Nicotine
- Product NDC
- 11673-456
- 11-digit product format
- 116730456
- Labeler code
- 11673
- Product ID
- 11673-456_71e79a44-f217-446f-b046-e02aca432e40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nicotine Polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA076777
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 2 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 |
|---|
| 11673-456 | UP AND UP NICOTINE (NICOTINE POLACRILEX) GUM, CHEWING [TARGET CORPORATION] | 11 | Legacy NDC | 20210414_9c39850b-19ed-4021-9677-08137a1c60dc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-456-78 | 11673045678 | 100 BLISTER PACK in 1 CARTON (11673-456-78) > 1 GUM, CHEWING in 1 BLISTER PACK | 100 blister pack | 2009-07-01 | 0000-00-00 | No | No | Current |