Nicotine
- Product NDC
- 63739-370
- 11-digit product format
- 637390370
- Labeler code
- 63739
- Product ID
- 63739-370_ae260e0f-2fda-4d9e-b086-a4f95f57f907
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nicotine Polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA079216
- Marketing category
- ANDA
- Marketing start
- 2020-04-27
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Cholinergic Nicotinic Agonist [EPC], Nicotine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63739-370 | NICOTINE (NICOTINE POLACRILEX) GUM, CHEWING [MCKESSON CORPORATION DBA SKY PACKAGING] | 6 | Legacy NDC | 20250309_17527002-5f98-438c-a3f2-5f4c7985ed1d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-370-10 | 63739037010 | 100 BLISTER PACK in 1 CARTON (63739-370-10) > 1 GUM, CHEWING in 1 BLISTER PACK | 100 blister pack | 2020-04-27 | 0000-00-00 | No | No | Current |