Nicotine
- Product NDC
- 63739-368
- 11-digit product format
- 637390368
- Labeler code
- 63739
- Product ID
- 63739-368_046a11a2-ea62-46f0-aa7e-787875b77df6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nicotine Polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA079038
- Marketing category
- ANDA
- Marketing start
- 2020-04-27
- 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 Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-368 | NICOTINE (NICOTINE POLACRILEX) GUM, CHEWING [MCKESSON CORPORATION DBA SKY PACKAGING] | 4 | Legacy NDC | 20250130_0d53243f-f1a7-4a1d-a93e-c0a8f05ed8df.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-368-10 | 63739036810 | 100 BLISTER PACK in 1 CARTON (63739-368-10) > 1 GUM, CHEWING in 1 BLISTER PACK | 100 blister pack | 2020-04-27 | 0000-00-00 | No | No | Current |