NICORETTE
- Product NDC
- 68151-5980
- 11-digit product format
- 681515980
- Labeler code
- 68151
- Product ID
- 68151-5980_62c04eb3-1970-4f9e-a94d-4e8fecbd0bd9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- nicotine polacrilex
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- NDA022360
- Marketing category
- NDA
- Marketing start
- 2010-03-01
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 68151-5980-1 | NICORETTE | 1 in 1 BLISTER PACK | LOZENGE | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-5980 | NICORETTE (NICOTINE POLACRILEX) LOZENGE [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20180207_e5f70dda-dd7a-49d4-992f-fb28b4bf0efc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-5980-1 | 68151598001 | 1 in 1 BLISTER PACK | Historical |