Moxifloxacin Hydrochloride Tablets, 400 Mg 70518-4312-00

Package NDC

70518-4312-00

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 18, 2025
Listing Expires: December 31, 2026
Application: ANDA208682

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Active Ingredients

Ingredient	Strength
Moxifloxacin Hydrochloride Monohydrate	400 mg/1

Drug Class

Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]

Selected Package

70518-4312-00Selected

7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0)