Primo APF
- Product NDC
- 69509-050
- 11-digit product format
- 695090050
- Labeler code
- 69509
- Product ID
- 69509-050_d607eca8-5abe-57dc-e053-2995a90a4396
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- Tri State Dental
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2013-09-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 6 g/454g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 69509-050-15 | Primo APF | 454 g in 1 BOTTLE, PLASTIC | GEL | 454 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69509-050 | PRIMO APF (SODIUM FLUORIDE) GEL [TRI STATE DENTAL] | 3 | Legacy NDC, 1 package rows | 20220121_1a1f0c6a-b162-4679-b222-550834538437.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 |
|---|
| 69509-050-15 | 69509005015 | 454 g in 1 BOTTLE, PLASTIC (69509-050-15) | 454 g | 2013-09-01 | 0000-00-00 | No | No | Current |