Moxifloxacin 33342-0322
Product NDC
33342-0322- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 2, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA209143
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Moxifloxacin Hydrochloride | 400 mg/1 |
Drug Class
Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (33342-322-07)
10 BLISTER PACK in 1 CARTON (33342-322-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK