NDC 68071-4122 – ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-4122

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 (6)

Package NDCDescriptionSince
68071-4122-110 TABLET in 1 BOTTLE (68071-4122-1)Oct 16, 2017
68071-4122-220 TABLET in 1 BOTTLE (68071-4122-2)Oct 16, 2017
68071-4122-330 TABLET in 1 BOTTLE (68071-4122-3)Oct 16, 2017
68071-4122-414 TABLET in 1 BOTTLE (68071-4122-4)Oct 16, 2017
68071-4122-660 TABLET in 1 BOTTLE (68071-4122-6)Oct 16, 2017
68071-4122-721 TABLET in 1 BOTTLE (68071-4122-7)Oct 16, 2017

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