NDC 72789-233 – Moxifloxacin

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

Human Prescription Drug

Product NDC72789-233

Product details

Brand name
Moxifloxacin
Generic name
Moxifloxacin
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076938
Marketed since
March 5, 2014
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Moxifloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
72789-233-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)Feb 15, 2022

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