Moxifloxacin 55111-0112
Product NDC
55111-0112- Manufacturer
- Dr. Reddy's Laboratories Limited
- 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
Quinolone Antimicrobial [EPC]Quinolones [CS]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (55111-112-01)
500 TABLET, FILM COATED in 1 BOTTLE (55111-112-05)
30 TABLET, FILM COATED in 1 BOTTLE (55111-112-30)
5 BLISTER PACK in 1 CARTON (55111-112-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-112-79)