Ciprofloxacin
NDC 70518-2837, Ciprofloxacin, tablet, film coated, from REMEDYREPACK INC..
- Product NDC
- 70518-2837
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076558
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2837 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CIPROFLOXACIN HYDROCHLORIDE250 mg/1
Pharmacologic classes
Cytochrome P450 1A2 Inhibitors [MoA]; Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-2837-4 | 70518283704 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-4) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c08b37c3-5f01-47ed-9508-02813bbd008b
Use it
Look up 70518-2837 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2837 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2837. 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.