up and up nicotine polacrilex
- Product NDC
- 11673-206
- 11-digit product format
- 116730206
- Labeler code
- 11673
- Product ID
- 11673-206_bd2bcc7f-d196-4f5b-84b1-31ec0dd22289
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nicotine Polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA078325
- Marketing category
- ANDA
- Marketing start
- 2011-10-06
- 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 |
|---|
| 11673-206 | UP AND UP NICOTINE POLACRILEX (NICOTINE POLACRILEX) GUM, CHEWING [TARGET CORPORATION] | 3 | Legacy NDC | 20210409_a4809ad2-d93b-4231-aba4-e3839be45f28.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-206-96 | 11673020696 | 170 BLISTER PACK in 1 CARTON (11673-206-96) > 1 GUM, CHEWING in 1 BLISTER PACK | 170 blister pack | 2017-11-28 | 0000-00-00 | No | No | Current |