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Ciprofloxacin and Dexamethasone

NDC 43598-326 · Dr. Reddy's Laboratories, Inc.

Generic nameCiprofloxacin and Dexamethasone
Dosage formSUSPENSION/ DROPS
RouteAURICULAR (OTIC)
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE, DEXAMETHASONE
Strength3; 1 mg/mL; mg/mL
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Marketing categoryANDA

Packages

43598-326-75 — 1 BOTTLE, DROPPER in 1 CARTON (43598-326-75) / 7.5 mL in 1 BOTTLE, DROPPER

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42708-088 — Ciprofloxacin, 42708-192 — ciprofloxacin, 43063-266 — Dexamethasone, 43063-410 — ciprofloxacin, 43063-547 — Ciprofloxacin, 43063-767 — ciprofloxacin, 43063-869 — ciprofloxacin, 43063-923 — Ciprofloxacin Hydrochloride, 43547-688 — Ciprofolxacin, 43547-689 — Ciprofolxacin, 47781-914 — dexamethasone, 47781-916 — dexamethasone, 50090-0570 — Neomycin sulfate, Polymyxin B Sulfate and Dexamethasone, 50090-0882 — Ciprofloxacin Hydrochloride, 50090-1135 — Tobramycin and Dexamethasone, 50090-1136 — Tobramycin and Dexamethasone, 50090-1648 — ciprofloxacin, 50090-1649 — ciprofloxacin, 50090-1754 — Ciprofloxacin Hydrochloride, 50090-1914 — Tobramycin and Dexamethasone, +390 more

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