NDC 33342-322 – Moxifloxacin

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

Human Prescription Drug

Product NDC33342-322

Product details

Brand name
Moxifloxacin
Generic name
Moxifloxacin
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209143
Marketed since
March 2, 2026
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Moxifloxacin →

Package NDC codes (2)

Package NDCDescriptionSince
33342-322-0730 TABLET, FILM COATED in 1 BOTTLE (33342-322-07)Mar 2, 2026
33342-322-1210 BLISTER PACK in 1 CARTON (33342-322-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKMar 2, 2026

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