NDC 66267-919 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC66267-919

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
September 10, 2004
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (5)

Package NDCDescriptionSince
66267-919-066 TABLET in 1 BOTTLE (66267-919-06)Jan 24, 2017
66267-919-1010 TABLET in 1 BOTTLE (66267-919-10)Jan 24, 2017
66267-919-2121 TABLET in 1 BOTTLE (66267-919-21)Jan 24, 2017
66267-919-3030 TABLET in 1 BOTTLE (66267-919-30)Jan 24, 2017
66267-919-6060 TABLET in 1 BOTTLE (66267-919-60)Jan 24, 2017

Other Ciprofloxacin products