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Ciprofloxacin Hydrochloride

NDC 83939-0002 · VERITYRX, LLC

Generic nameCiprofloxacin Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE
Strength500 mg/1
Pharmacologic classCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

83939-0002-1 — 1 TABLET, FILM COATED in 1 POUCH (83939-0002-1)

83939-0002-2 — 50 POUCH in 1 BOX, UNIT-DOSE (83939-0002-2) / 1 TABLET, FILM COATED in 1 POUCH

83939-0002-3 — 100 POUCH in 1 BOX, UNIT-DOSE (83939-0002-3) / 1 TABLET, FILM COATED in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

80425-0192 — Ciprofloxacin HCL, 80425-0492 — Ciprofolxacin, 80425-0493 — Ciprofloxacin Hydrochloride, 80425-0499 — Ciprofloxacin, 82804-130 — Ciprofolxacin, 82804-256 — Ciprofolxacin, 82804-260 — Ciprofloxacin Hydrochloride, 82868-070 — Ciprofloxacin Hydrochloride, 82868-102 — ciprofloxacin, 83008-078 — Ciprofolxacin, 85293-002 — ciprofloxacin, 85293-003 — ciprofloxacin, 85293-004 — ciprofloxacin, 85534-0047 — Ciprofloxacin Hydrochloride, 85534-0069 — Ciprofloxacin Hydrochloride, 85534-0075 — Ciprofloxacin, 85534-0081 — Ciprofloxacin Hydrochloride, 85766-023 — Ciprofloxacin, 85766-099 — Ciprofolxacin, 85766-100 — Ciprofolxacin, +195 more

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