NDC 72789-118 – Ciprofloxacin

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

Human Prescription Drug

Product NDC72789-118

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 (2)

Package NDCDescriptionSince
72789-118-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-118-01)Sep 16, 2020
72789-118-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-118-20)Sep 16, 2020

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