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Ciprofloxacin and Dexamethasone

NDC 16714-628 · NorthStar RxLLC

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

16714-628-01 — 1 BOTTLE, DROPPER in 1 CARTON (16714-628-01) / 7.5 mL in 1 BOTTLE, DROPPER

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0832-1430 — Ciprofloxacin Hydrochloride and Dexamethasone, 0904-7243 — ciprofloxacin, 0904-7266 — dexamethasone, 0904-7267 — dexamethasone, 0904-7444 — dexamethasone, 10135-795 — Dexamethasone, 16252-515 — Ciprofloxacin, 16571-411 — ciprofloxacin, 16571-412 — ciprofloxacin, 16571-413 — ciprofloxacin, 24208-295 — Tobramycin and Dexamethasone, 24208-795 — Neomycin Sulfate, Polymyxin B Sulfate, and Dexamethasone, 24208-830 — Neomycin sulfate, Polymyxin B Sulfate and Dexamethasone, 42708-088 — Ciprofloxacin, 42708-192 — ciprofloxacin, 43063-266 — Dexamethasone, 43063-410 — ciprofloxacin, 43063-547 — Ciprofloxacin, 43063-767 — ciprofloxacin, 43063-869 — ciprofloxacin, +390 more

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