NDC 72789-108 – Ciprofloxacin

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

Human Prescription Drug

Product NDC72789-108

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, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (6)

Package NDCDescriptionSince
72789-108-022 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-02)Apr 5, 2022
72789-108-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-10)Dec 9, 2021
72789-108-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-14)Jul 21, 2021
72789-108-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-20)Dec 30, 2020
72789-108-2828 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-28)May 5, 2022
72789-108-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-108-30)Dec 9, 2020

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