Moxifloxacin 72789-0233
Product NDC
72789-0233- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 5, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA076938
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Moxifloxacin Hydrochloride | 400 mg/1 |
Drug Class
Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(1)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)