NDC 85766-099 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC85766-099

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
Sportpharm LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
October 1, 2023
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (6)

Package NDCDescriptionSince
85766-099-01100 TABLET in 1 BOTTLE (85766-099-01)Oct 10, 2025
85766-099-1010 TABLET in 1 BOTTLE (85766-099-10)Oct 10, 2025
85766-099-2020 TABLET in 1 BOTTLE (85766-099-20)Oct 10, 2025
85766-099-3030 TABLET in 1 BOTTLE (85766-099-30)Oct 10, 2025
85766-099-6060 TABLET in 1 BOTTLE (85766-099-60)Oct 10, 2025
85766-099-9090 TABLET in 1 BOTTLE (85766-099-90)Oct 10, 2025

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