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Ciprofloxacin

NDC 43063-547 · PD-Rx Pharmaceuticals, Inc.

Generic nameCiprofloxacin
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

43063-547-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-547-01)

43063-547-20 — 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-547-20)

43063-547-82 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-547-82)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0832-1430 — Ciprofloxacin Hydrochloride and Dexamethasone, 0904-7243 — ciprofloxacin, 16252-515 — Ciprofloxacin, 16571-411 — ciprofloxacin, 16571-412 — ciprofloxacin, 16571-413 — ciprofloxacin, 16714-628 — Ciprofloxacin and Dexamethasone, 42708-088 — Ciprofloxacin, 42708-192 — ciprofloxacin, 43063-410 — ciprofloxacin, 43063-767 — ciprofloxacin, 43063-869 — ciprofloxacin, 43063-923 — Ciprofloxacin Hydrochloride, 43547-688 — Ciprofolxacin, 43547-689 — Ciprofolxacin, 43598-326 — Ciprofloxacin and Dexamethasone, 50090-0882 — Ciprofloxacin Hydrochloride, 50090-1648 — ciprofloxacin, 50090-1649 — ciprofloxacin, 50090-1754 — 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.