NDC 68071-2404 – Ciprofloxacin

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

Human Prescription Drug

Product NDC68071-2404

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
August 12, 2020
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (3)

Package NDCDescriptionSince
68071-2404-22 TABLET, COATED in 1 BOTTLE (68071-2404-2)May 21, 2021
68071-2404-44 TABLET, COATED in 1 BOTTLE (68071-2404-4)May 21, 2021
68071-2404-66 TABLET, COATED in 1 BOTTLE (68071-2404-6)May 21, 2021

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