NDC 66267-716 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC66267-716

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 (3)

Package NDCDescriptionSince
66267-716-022 TABLET in 1 BOTTLE (66267-716-02)Dec 30, 2016
66267-716-044 TABLET in 1 BOTTLE (66267-716-04)Dec 30, 2016
66267-716-066 TABLET in 1 BOTTLE (66267-716-06)Dec 30, 2016

Other Ciprofloxacin products