Ciprofloxacin Hydrochloride
NDC 68071-3351, Ciprofloxacin Hydrochloride, solution/ drops, from NuCare Pharmaceuticals,Inc..
- Product NDC
- 68071-3351
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA019992
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3351 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CIPROFLOXACIN HYDROCHLORIDE3 mg/mL
Pharmacologic classes
Cytochrome P450 1A2 Inhibitors [MoA]; Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-3351-3 | 68071335103 | 10 mL in 1 BOX (68071-3351-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/54c73290-bd89-3453-e054-00144ff88e88
Use it
Look up 68071-3351 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3351 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-3351. 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.