NDC 50090-7665 – Moxifloxacin Hydrochloride

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

Human Prescription Drug

Product NDC50090-7665

Product details

Brand name
Moxifloxacin Hydrochloride
Generic name
Moxifloxacin Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202632
Marketed since
March 4, 2014
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50090-7665-030 TABLET, FILM COATED in 1 BOTTLE (50090-7665-0)Oct 1, 2025

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