NDC 72789-193 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72789-193

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076558
Marketed since
June 9, 2004
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
72789-193-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-06)Jun 14, 2021
72789-193-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-10)Dec 22, 2022
72789-193-1212 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-12)Oct 11, 2021
72789-193-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-14)Nov 11, 2021
72789-193-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-193-20)Jun 14, 2021

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