NDC 65862-603 – Moxifloxacin Hydrochloride

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

Human Prescription Drug

Product NDC65862-603

Product details

Brand name
Moxifloxacin Hydrochloride
Generic name
Moxifloxacin hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202632
Marketed since
March 4, 2014
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
65862-603-3030 TABLET, FILM COATED in 1 BOTTLE (65862-603-30)Mar 4, 2014
65862-603-5550 BLISTER PACK in 1 BOX, UNIT-DOSE (65862-603-55) / 1 TABLET, FILM COATED in 1 BLISTER PACK (65862-603-10)Mar 4, 2014
65862-603-991000 TABLET, FILM COATED in 1 BOTTLE (65862-603-99)Mar 4, 2014

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