NDC 50090-7297 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-7297

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
A-S Medication Solutions
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
50090-7297-06 TABLET in 1 BOTTLE (50090-7297-0)Oct 10, 2024
50090-7297-114 TABLET in 1 BOTTLE (50090-7297-1)Oct 10, 2024
50090-7297-210 TABLET in 1 BOTTLE (50090-7297-2)Oct 10, 2024
50090-7297-33 TABLET in 1 BOTTLE (50090-7297-3)Oct 10, 2024

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