Sodium Fluoride Chewable
- Product NDC
- 71335-2724
- 11-digit product format
- 713352724
- Labeler code
- 71335
- Product ID
- 71335-2724_31cdf96a-0470-4d6e-b78d-0be36f1c4300
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-08-17
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Fluoride Chewable
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 315213 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2724-1 | Sodium Fluoride Chewable | 120 in 1 BOTTLE | TABLET | 120 | | 101 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2724-1 | 71335272401 | 120 TABLET in 1 BOTTLE (71335-2724-1) | 120 tablet | 2025-07-29 | No | No | Historical |