NDC 70518-4458 – Moxifloxacin Hydrochloride

Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-4458

Product details

Brand name
Moxifloxacin Hydrochloride
Generic name
Moxifloxacin Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202632
Marketed since
August 27, 2025
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Moxifloxacin Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4458-07 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4458-0)Aug 27, 2025

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