Ciprofloxacin
NDC 58657-676, Ciprofloxacin, tablet, coated, from Method Pharmaceuticals, LLC.
- Product NDC
- 58657-676
- Status
- Listed
- Labeler
- Method Pharmaceuticals, LLC
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208921
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/58657-676 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CIPROFLOXACIN HYDROCHLORIDE500 mg/1
Pharmacologic classes
Cytochrome P450 1A2 Inhibitors [MoA]; Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 58657-676-01 | 58657067601 | 100 TABLET, COATED in 1 BOTTLE (58657-676-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/acb03e72-ce94-58c5-e053-2a95a90a683a
Use it
Look up 58657-676 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/58657-676 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 58657-676. 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.