Sodium Fluoride
NDC 58657-322, Sodium Fluoride, solution/ drops, from Method Pharmaceuticals, LLC.
- Product NDC
- 58657-322
- Status
- Listed
- Labeler
- Method Pharmaceuticals, LLC
- Dosage form
- SOLUTION/ DROPS
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/58657-322 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.5 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 58657-322-50 | 58657032250 | 50 mL in 1 BOTTLE, DROPPER (58657-322-50) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/35dcc144-130d-4ec7-a266-c084008ac70cNADAC price for package 58657032250
GET /v1/drugs/nadac/58657032250
Use it
Look up 58657-322 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/58657-322 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 58657-322. 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.