Ciprofloxacin Hydrochloride
NDC 69367-387, Ciprofloxacin Hydrochloride, tablet, film coated, from Westminster Pharmaceuticals, LLC.
- Product NDC
- 69367-387
- Status
- Listed
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076593
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69367-387 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CIPROFLOXACIN HYDROCHLORIDE750 mg/1
Pharmacologic classes
Cytochrome P450 1A2 Inhibitors [MoA]; Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69367-387-50 | 69367038750 | 50 TABLET, FILM COATED in 1 BOTTLE (69367-387-50) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c47250c2-bece-46b5-8b3b-b7c97d9005d8NADAC price for package 69367038750
GET /v1/drugs/nadac/69367038750
Use it
Look up 69367-387 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69367-387 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69367-387. 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.