Ciprofloxacin Hydrochloride 68071-4139
Product NDC
68071-4139- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- May 7, 2004
- Listing Expires
- December 31, 2026
- Application
- NDA019992
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ciprofloxacin Hydrochloride | 3 mg/mL |
Drug Class
Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(1)
5 mL in 1 BOX (68071-4139-5)