Guaifenesin
NDC 58657-508, Guaifenesin, liquid, from Method Pharmaceuticals, LLC.
- Product NDC
- 58657-508
- Status
- Listed
- Labeler
- Method Pharmaceuticals, LLC
- Dosage form
- LIQUID
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M012
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/58657-508 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GUAIFENESIN100 mg/5mL
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 58657-508-16 | 58657050816 | 473 mL in 1 BOTTLE (58657-508-16) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
NADAC price for package 58657050816
GET /v1/drugs/nadac/58657050816
Use it
Look up 58657-508 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/58657-508 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 58657-508. 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.