sunmark nicotine
- Product NDC
- 70677-0170
- 11-digit product format
- 706770170
- Labeler code
- 70677
- Product ID
- 70677-0170_29ae0e2a-9161-491e-8f9f-65e83717ed64
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- nicotine polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA206393
- Marketing category
- ANDA
- Marketing start
- 2022-12-15
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 4 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6M3C89ZY6R | NICOTINE | 54-11-5 | NICOTINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70677-0170-0 | 70677017000 | 110 BLISTER PACK in 1 CARTON (70677-0170-0) > 1 GUM, CHEWING in 1 BLISTER PACK | 110 blister pack | 2022-12-15 | 0000-00-00 | No | No | Current |