NDC 72189-623 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-623

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Direct_Rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
May 14, 2025
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (3)

Package NDCDescriptionSince
72189-623-1010 TABLET in 1 BOTTLE (72189-623-10)May 14, 2025
72189-623-1414 TABLET in 1 BOTTLE (72189-623-14)May 14, 2025
72189-623-2020 TABLET in 1 BOTTLE (72189-623-20)May 14, 2025

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