Sodium Fluoride Chewable
NDC 58657-160, Sodium Fluoride, tablet, from Method Pharmaceuticals, LLC.
- Product NDC
- 58657-160
- Status
- Listed
- Labeler
- Method Pharmaceuticals, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/58657-160 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.25 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 58657-160-12 | 58657016012 | 120 TABLET in 1 BOTTLE (58657-160-12) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e2061541-bf1c-4ee3-afde-36894394dbeaNADAC price for package 58657016012
GET /v1/drugs/nadac/58657016012
Use it
Look up 58657-160 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/58657-160 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 58657-160. 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.