NDC 51407-165 – Ciprofloxacin

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

Human Prescription Drug

Product NDC51407-165

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076126
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 (3)

Package NDCDescriptionSince
51407-165-01100 TABLET, FILM COATED in 1 BOTTLE (51407-165-01)Oct 5, 2021
51407-165-2020 TABLET, FILM COATED in 1 BOTTLE (51407-165-20)Feb 6, 2023
51407-165-2828 TABLET, FILM COATED in 1 BOTTLE (51407-165-28)Jan 24, 2024

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