NDC 55111-112 – Moxifloxacin

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

Human Prescription Drug

Product NDC55111-112

Product details

Brand name
Moxifloxacin
Generic name
Moxifloxacin
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076938
Marketed since
March 5, 2014
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Moxifloxacin →

Package NDC codes (4)

Package NDCDescriptionSince
55111-112-01100 TABLET, FILM COATED in 1 BOTTLE (55111-112-01)Mar 5, 2014
55111-112-05500 TABLET, FILM COATED in 1 BOTTLE (55111-112-05)Mar 5, 2014
55111-112-3030 TABLET, FILM COATED in 1 BOTTLE (55111-112-30)Mar 5, 2014
55111-112-665 BLISTER PACK in 1 CARTON (55111-112-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-112-79)Mar 5, 2014

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