NDC 68071-2269 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68071-2269

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076794
Marketed since
November 1, 2006
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
68071-2269-44 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2269-4)Sep 28, 2020

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