Flavoxate Hydrochloride
NDC 24658-720, Flavoxate Hydrochloride, tablet, from PuraCap Laboratories LLC dba Blu Pharmaceuticals.
- Product NDC
- 24658-720
- Status
- Listed
- Labeler
- PuraCap Laboratories LLC dba Blu Pharmaceuticals
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076835
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/24658-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLAVOXATE HYDROCHLORIDE100 mg/1
Pharmacologic classes
Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 24658-720-01 | 24658072001 | 100 TABLET in 1 BOTTLE (24658-720-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f6a06eda-2480-4c0d-8d1e-9e3e89d3ee88
Use it
Look up 24658-720 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/24658-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 24658-720. 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.