NDC 72789-511 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72789-511

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
February 9, 2024
Marketing end
February 29, 2028
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (4)

Package NDCDescriptionSince
72789-511-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-10)Aug 27, 2025
72789-511-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-14)Jul 31, 2025
72789-511-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-20)Sep 12, 2025
72789-511-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-30)Jun 2, 2025

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