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Moxifloxacin

NDC 80425-0379 · Advanced Rx Pharmacy of Tennessee, LLC

Generic nameMoxifloxacin
Dosage formSOLUTION/ DROPS
RouteOPHTHALMIC
Active ingredient(s)MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
Strength5 mg/mL
Pharmacologic classFluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

80425-0379-1 — 1 BOTTLE in 1 CARTON (80425-0379-1) / 3 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-321 — moxifloxacin, 60505-0582 — moxifloxacin, 67296-2129 — Moxifloxacin, 68180-422 — Moxifloxacin, 70518-4312 — Moxifloxacin Hydrochloride Tablets, 400 mg, 72162-2107 — moxifloxacin, 72189-321 — MOXIFLOXACIN, 72205-001 — Moxifloxacin Hydrochloride Tablets, 400 mg, 72789-080 — Moxifloxacin Hydrochloride Tablets, 400 mg, 80425-0239 — Moxifloxacin

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels