Ciprofloxacin
NDC 59651-873, Ciprofloxacin Hydrochloride, tablet, film coated, from Aurobindo Pharma Limited.
- Product NDC
- 59651-873
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077859
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-873 \ -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 |
|---|---|---|
| 59651-873-50 | 59651087350 | 50 TABLET, FILM COATED in 1 BOTTLE (59651-873-50) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7041828f-d4ec-4813-bcac-cb335c6c312aNADAC price for package 59651087350
GET /v1/drugs/nadac/59651087350
Use it
Look up 59651-873 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-873 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-873. 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.