Moxifloxacin Hydrochloride 57237-0156
Product NDC
57237-0156- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 4, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA202632
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Moxifloxacin Hydrochloride | 400 mg/1 |
Drug Class
Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (57237-156-30)