NDC 50268-576 – Moxifloxacin Hydrochloride

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

Human Prescription Drug

Product NDC50268-576

Product details

Brand name
Moxifloxacin Hydrochloride
Generic name
Moxifloxacin Hydrochloride
Labeler
AvPAK
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202632
Marketed since
July 22, 2016
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50268-576-1330 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-576-13) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-576-11)Jul 22, 2016

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