NDC 50090-1649 – ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-1649

Product details

Brand name
ciprofloxacin
Generic name
ciprofloxacin
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
September 10, 2004
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (2)

Package NDCDescriptionSince
50090-1649-020 TABLET in 1 BOTTLE (50090-1649-0)Jan 19, 2015
50090-1649-114 TABLET in 1 BOTTLE (50090-1649-1)Oct 31, 2023

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