NDC 72789-519 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-519

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
PD-Rx Pharmaceuticals, Inc.
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 (5)

Package NDCDescriptionSince
72789-519-066 TABLET in 1 BOTTLE, PLASTIC (72789-519-06)Sep 18, 2025
72789-519-1010 TABLET in 1 BOTTLE, PLASTIC (72789-519-10)Aug 22, 2025
72789-519-1212 TABLET in 1 BOTTLE, PLASTIC (72789-519-12)Oct 24, 2025
72789-519-1414 TABLET in 1 BOTTLE, PLASTIC (72789-519-14)Jul 31, 2025
72789-519-2020 TABLET in 1 BOTTLE, PLASTIC (72789-519-20)Sep 10, 2025

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