NDC 68071-3699 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3699

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
NuCare Pharmaceutical, 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 (4)

Package NDCDescriptionSince
68071-3699-110 TABLET in 1 BOTTLE (68071-3699-1)Aug 1, 2025
68071-3699-220 TABLET in 1 BOTTLE (68071-3699-2)Dec 19, 2025
68071-3699-330 TABLET in 1 BOTTLE (68071-3699-3)Oct 14, 2024
68071-3699-66 TABLET in 1 BOTTLE (68071-3699-6)Dec 11, 2024

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