NDC 80425-0095

Cipro

Ciprofloxacin Hcl 500mg

Cipro is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Advanced Rx Pharmacy Of Tennessee, Llc. The primary component is Ciprofloxacin Hydrochloride.

• Product ID: 80425-0095_b440e65e-88f4-f864-e053-2a95a90a1e77
• NDC: 80425-0095
• Product Type: Human Prescription Drug
• Proprietary Name: Cipro
• Generic Name: Ciprofloxacin Hcl 500mg
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2007-04-26
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077859
• Labeler Name: Advanced Rx Pharmacy of Tennessee, LLC
• Substance Name: CIPROFLOXACIN HYDROCHLORIDE
• Active Ingredient Strength: 500 mg/1
• Pharm Classes: Quinolone Antimicrobial [EPC],Quinolones [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 80425-0095-2

30 TABLET, FILM COATED in 1 BOTTLE (80425-0095-2)

• Marketing Start Date: 2007-04-26
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Cipro" or generic name "Ciprofloxacin Hcl 500mg"

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
50419-754	Cipro	ciprofloxacin hydrochloride
50419-758	Cipro	ciprofloxacin hydrochloride
50419-759	Cipro	ciprofloxacin
50419-773	Cipro	ciprofloxacin
50419-777	Cipro	ciprofloxacin
50419-788	Cipro	ciprofloxacin
50419-789	Cipro	ciprofloxacin
80425-0095	Cipro	Cipro