Moxifloxacin Hydrochloride 57237-0156-30

Package NDC

57237-0156-30

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]

Selected Package

57237-0156-30Selected

30 TABLET, FILM COATED in 1 BOTTLE (57237-156-30)