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Ciprofloxacin

NDC 82804-130 · Proficient Rx LP

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

Packages

82804-130-06 — 6 TABLET in 1 BOTTLE (82804-130-06)

82804-130-10 — 10 TABLET in 1 BOTTLE (82804-130-10)

82804-130-14 — 14 TABLET in 1 BOTTLE (82804-130-14)

82804-130-20 — 20 TABLET in 1 BOTTLE (82804-130-20)

82804-130-30 — 30 TABLET in 1 BOTTLE (82804-130-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76420-214 — Ciprofloxacin, 76420-273 — ciprofloxacin hydrochloride and hydrocortisone, 76420-588 — Ciprofloxacin, 76420-928 — Ciprofolxacin, 76420-929 — Ciprofolxacin, 76420-942 — Ciprofloxacin Hydrochloride, 80425-0192 — Ciprofloxacin HCL, 80425-0492 — Ciprofolxacin, 80425-0493 — Ciprofloxacin Hydrochloride, 80425-0499 — Ciprofloxacin, 82804-256 — Ciprofolxacin, 82804-260 — Ciprofloxacin Hydrochloride, 82868-070 — Ciprofloxacin Hydrochloride, 82868-102 — ciprofloxacin, 83008-078 — Ciprofolxacin, 83939-0002 — Ciprofloxacin Hydrochloride, 85293-002 — ciprofloxacin, 85293-003 — ciprofloxacin, 85293-004 — ciprofloxacin, 85534-0047 — Ciprofloxacin Hydrochloride, +195 more

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