NDC 62135-014 – Moxifloxacin

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

Human Prescription Drug

Product NDC62135-014

Product details

Brand name
Moxifloxacin
Generic name
Moxifloxacin
Labeler
Chartwell RX, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207285
Marketed since
February 13, 2017
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Moxifloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
62135-014-3030 TABLET, FILM COATED in 1 BOTTLE (62135-014-30)Aug 11, 2026

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