NDC 0078-0855

CIPRO HC

Ciprofloxacin Hydrochloride And Hydrocortisone

CIPRO HC is a Auricular (otic) Suspension/ Drops in the Human Prescription Drug category. It is labeled and distributed by Novartis Pharmaceuticals Corporation. The primary component is Ciprofloxacin Hydrochloride; Hydrocortisone.

• Product ID: 0078-0855_eff6ee40-6e52-4f61-b54d-edc612543f71
• NDC: 0078-0855
• Product Type: Human Prescription Drug
• Proprietary Name: CIPRO HC
• Generic Name: Ciprofloxacin Hydrochloride And Hydrocortisone
• Dosage Form: Suspension/ Drops
• Route of Administration: AURICULAR (OTIC)
• Marketing Start Date: 1999-03-15
• Marketing Category: NDA /
• Application Number: NDA020805
• Labeler Name: Novartis Pharmaceuticals Corporation
• Substance Name: CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE
• Active Ingredient Strength: 2 mg/mL; mg/mL
• Pharm Classes: Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Quinolone Antimicrobial [EPC], Quinolones [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0078-0855-26

10 mL in 1 BOTTLE (0078-0855-26)

• Marketing Start Date: 2022-03-08
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "CIPRO HC" or generic name "Ciprofloxacin Hydrochloride And Hydrocortisone"

NDC	Brand Name	Generic Name
0065-8531	CIPRO	ciprofloxacin hydrochloride and hydrocortisone
0078-0855	CIPRO	ciprofloxacin hydrochloride and hydrocortisone
50090-1656	CIPRO	ciprofloxacin hydrochloride and hydrocortisone
50090-6043	CIPRO	ciprofloxacin hydrochloride and hydrocortisone
76420-273	CIPRO	ciprofloxacin hydrochloride and hydrocortisone