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MOXIFLOXACIN

NDC 68180-421 · Lupin Pharmaceuticals, Inc.

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

Packages

68180-421-01 — 3 mL in 1 BOTTLE (68180-421-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63323-850 — MOXIFLOXACIN HYDROCHLORIDE, 63629-8357 — Moxifloxacin, 65862-603 — moxifloxacin hydrochloride, 65862-840 — MOXIFLOXACIN, 66298-8507 — MOXIFLOXACIN HYDROCHLORIDE, 67296-2222 — Moxifloxacin, 67296-2232 — Moxifloxacin Hydrochloride, 67457-323 — MOXIFLOXACIN HYDROCHLORIDE, 68083-210 — Moxifloxacin Ophthalmic, 68084-722 — Moxifloxacin Hydrochloride, 70069-081 — Moxifloxacin Hydrochloride, 70518-3738 — moxifloxacin hydrochloride, 70518-4458 — Moxifloxacin Hydrochloride, 70756-638 — Moxifloxacin, 71335-2329 — moxifloxacin hydrochloride, 71335-2815 — Moxifloxacin Hydrochloride, 72189-334 — MOXIFLOXACIN, 72266-158 — Moxifloxacin Ophthalmic, 72789-037 — moxifloxacin hydrochloride, 72789-038 — moxifloxacin hydrochloride, +25 more

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