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Ciprofloxacin Hydrochloride

NDC 50090-7848 · A-S Medication Solutions

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

50090-7848-1 — 14 TABLET, FILM COATED in 1 BOTTLE (50090-7848-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-3791 — Ciprofloxacin Hydrochloride, 50090-3852 — Ciprofloxacin Hydrochloride, 50090-4217 — Ciprofloxacin, 50090-4600 — Ciprofloxacin Hydrochloride, 50090-5373 — Ciprofloxacin Hydrochloride, 50090-6043 — ciprofloxacin hydrochloride and hydrocortisone, 50090-7297 — Ciprofolxacin, 50090-7581 — Ciprofloxacin Hydrochloride, 50090-7631 — ciprofloxacin hydrochloride and hydrocortisone, 50090-7843 — Ciprofloxacin Hydrochloride, 50419-754 — ciprofloxacin hydrochloride, 50419-758 — ciprofloxacin hydrochloride, 51407-165 — Ciprofloxacin Hydrochloride, 51407-775 — Ciprofloxacin Hydrochloride, 51407-776 — Ciprofloxacin Hydrochloride, 51655-086 — Ciprofloxacin, 51655-216 — Ciprofloxacin Hydrochloride, 51655-490 — Ciprofloxacin, 53746-831 — Ciprofloxacin and Dexamethasone, 54348-662 — CIPROFLOXACIN, +195 more

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