Sunmark Nicotine
- Product NDC
- 50090-4265
- 11-digit product format
- 500904265
- Labeler code
- 50090
- Product ID
- 50090-4265_b74ec626-ad1c-417b-bd32-97c3c4b714e2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nicotine Polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078326
- Marketing category
- ANDA
- Marketing start
- 2005-06-23
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4265-0 | Sunmark Nicotine | 1 in 1 BLISTER PACK | GUM, CHEWING | 1 | | 3 |
| 50090-4265-0 | Sunmark Nicotine | 110 in 1 CARTON | GUM, CHEWING | 110 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4265 | SUNMARK NICOTINE (NICOTINE POLACRILEX) GUM, CHEWING [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20210418_bb379d6c-637e-4577-88a7-53508de4f53d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4265-0 | 50090426500 | 110 BLISTER PACK in 1 CARTON (50090-4265-0) > 1 GUM, CHEWING in 1 BLISTER PACK | 110 blister pack | 2019-04-12 | 0000-00-00 | No | No | Current |