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Moxifloxacin Hydrochloride

NDC 50090-6609 · A-S Medication Solutions

Generic nameMoxifloxacin Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)MOXIFLOXACIN HYDROCHLORIDE
Strength400 mg/1
Pharmacologic classFluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

50090-6609-0 — 10 TABLET, FILM COATED in 1 BOTTLE (50090-6609-0)

50090-6609-1 — 7 TABLET, FILM COATED in 1 BOTTLE (50090-6609-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0781-7135 — moxifloxacin hydrochloride, 0832-1410 — Moxifloxacin Hydrochloride, 0904-7407 — moxifloxacin hydrochloride, 16714-643 — MOXIFLOXACIN, 31722-845 — Moxifloxacin, 33342-322 — Moxifloxacin, 46708-505 — Moxifloxacin ophthalmic solution, 50090-4781 — Moxifloxacin ophthalmic, 50090-6248 — Moxifloxacin Ophthalmic, 50090-6357 — Moxifloxacin, 50090-7244 — moxifloxacin hydrochloride, 50090-7665 — Moxifloxacin Hydrochloride, 50090-8029 — MOXIFLOXACIN, 50268-576 — Moxifloxacin Hydrochloride, 55111-112 — Moxifloxacin, 57237-156 — Moxifloxacin Hydrochloride, 62135-014 — Moxifloxacin, 62332-505 — Moxifloxacin ophthalmic solution, 63323-850 — MOXIFLOXACIN HYDROCHLORIDE, 63629-8357 — Moxifloxacin, +25 more

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