Burkhart
- Product NDC
- 43498-201
- 11-digit product format
- 434980201
- Labeler code
- 43498
- Product ID
- 43498-201_d70dc1ee-062b-64d4-e053-2995a90a7559
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Stannous Fluoride
- Dosage form
- CONCENTRATE
- Route
- DENTAL
- Labeler
- Burkhart Dental Supply Inc
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2013-02-01
- Substance
- STANNOUS FLUORIDE
- Active strength
- .3408 g/284g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Burkhart
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| STANNOUS FLUORIDE | .3408 g/284g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3FTR44B32Q |
| Rxcui | 583459 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43498-201-10 | Burkhart | 284 g in 1 BOTTLE, PLASTIC | CONCENTRATE | 284 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43498-201 | BURKHART (STANNOUS FLUORIDE) CONCENTRATE [BURKHART DENTAL SUPPLY INC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20220203_47142a7d-3095-4ea6-b977-80e9f2cc8958.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 |
|---|
| 43498-201-10 | 43498020110 | 284 g in 1 BOTTLE, PLASTIC (43498-201-10) | 284 g | 2013-09-01 | 0000-00-00 | No | No | Current |