NDC 0781-6186 – Ciprofloxacin and Dexamethasone

Ciprofloxacin Hydrochloride 3 mg/mL; Dexamethasone 1 mg/mL · Suspension/ Drops · Auricular (otic)

Human Prescription Drug 1 recall

Product NDC0781-6186

Product details

Brand name
Ciprofloxacin and Dexamethasone
Generic name
Ciprofloxacin and dexamethasone
Labeler
Sandoz Inc
Dosage form
Suspension/ Drops
Route
Auricular (otic)
Marketing category
NDA AUTHORIZED GENERIC · NDA021537
Marketed since
August 10, 2020
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid; Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin and Dexamethasone →

Package NDC codes (1)

Package NDCDescriptionSince
0781-6186-671 BOTTLE, DROPPER in 1 CARTON (0781-6186-67) / 7.5 mL in 1 BOTTLE, DROPPERAug 10, 2020

Recalls mentioning this NDC

Other Ciprofloxacin and Dexamethasone products