NDC 0904-7407 – Moxifloxacin Hydrochloride

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

Human Prescription Drug

Product NDC0904-7407

Product details

Brand name
Moxifloxacin Hydrochloride
Generic name
Moxifloxacin hydrochloride
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202632
Marketed since
March 8, 2024
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0904-7407-0430 BLISTER PACK in 1 CARTON (0904-7407-04) / 1 TABLET, FILM COATED in 1 BLISTER PACKMar 8, 2024
0904-7407-0650 BLISTER PACK in 1 CARTON (0904-7407-06) / 1 TABLET, FILM COATED in 1 BLISTER PACKMar 8, 2024

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