Moxifloxacin Hydrochloride 70069-0081
Product NDC
70069-0081- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- November 25, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA209698
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Moxifloxacin Hydrochloride | 5 mg/mL |
Drug Class
Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(1)
1 BOTTLE in 1 CARTON (70069-081-01) / 3 mL in 1 BOTTLE