Fluoride
NDC 75826-163, Sodium Fluoride, tablet, chewable, from WINDER LABORATORIES, LLC.
- Product NDC
- 75826-163
- Status
- Listed
- Labeler
- WINDER LABORATORIES, LLC
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/75826-163 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.25 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 75826-163-20 | 75826016320 | 120 TABLET, CHEWABLE in 1 BOTTLE (75826-163-20) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/0df8f1aa-f3ef-9f59-e063-6294a90a0666NADAC price for package 75826016320
GET /v1/drugs/nadac/75826016320
Use it
Look up 75826-163 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/75826-163 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 75826-163. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.