Moxifloxacin Hydrochloride 50268-0576
Product NDC
50268-0576- Manufacturer
- Avpak
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 22, 2016
- Listing Expires
- December 31, 2027
- 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 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-576-13) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-576-11)