NDC 68071-3610 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3610

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
October 1, 2023
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
68071-3610-110 TABLET in 1 BOTTLE (68071-3610-1)Jun 17, 2024
68071-3610-220 TABLET in 1 BOTTLE (68071-3610-2)Jun 17, 2024
68071-3610-414 TABLET in 1 BOTTLE (68071-3610-4)Jun 17, 2024
68071-3610-66 TABLET in 1 BOTTLE (68071-3610-6)Aug 5, 2025
68071-3610-828 TABLET in 1 BOTTLE (68071-3610-8)Dec 3, 2025

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