Fluoride
- Product NDC
- 75826-164
- 11-digit product format
- 758260164
- Labeler code
- 75826
- Product ID
- 75826-164_47a68277-53e0-538f-e063-6394a90aa82c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- WINDER LABORATORIES, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2024-01-01
- Substance
- SODIUM FLUORIDE
- Active strength
- .5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluoride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 198215, 313036, 315213 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75826-164-20 | Fluoride | 120 in 1 BOTTLE | TABLET, CHEWABLE | 120 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75826-164 | FLUORIDE (SODIUM FLUORIDE) TABLET, CHEWABLE [WINDER LABORATORIES, LLC] | 1 | Current NDC, 1 package rows | 20240103_0df8f1aa-f3ef-9f59-e063-6294a90a0666.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 75826-164-20 | 75826016420 | 120 TABLET, CHEWABLE in 1 BOTTLE (75826-164-20) | 2024-01-01 | No | No | Current |