Ciprofloxacin Hydrochloride 83939-0002
Product NDC
83939-0002- Manufacturer
- Verityrx, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 23, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA076593
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ciprofloxacin Hydrochloride | 500 mg/1 |
Drug Class
Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(3)
1 TABLET, FILM COATED in 1 POUCH (83939-0002-1)
50 POUCH in 1 BOX, UNIT-DOSE (83939-0002-2) / 1 TABLET, FILM COATED in 1 POUCH
100 POUCH in 1 BOX, UNIT-DOSE (83939-0002-3) / 1 TABLET, FILM COATED in 1 POUCH