NDC 63629-3868 – Ciprofloxacin

Ciprofloxacin Hydrochloride 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63629-3868

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Bryant Ranch Prepack
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 (7)

Package NDCDescriptionSince
63629-3868-120 TABLET, FILM COATED in 1 BOTTLE (63629-3868-1)Oct 30, 2008
63629-3868-228 TABLET, FILM COATED in 1 BOTTLE (63629-3868-2)Jun 12, 2009
63629-3868-314 TABLET, FILM COATED in 1 BOTTLE (63629-3868-3)Apr 23, 2013
63629-3868-430 TABLET, FILM COATED in 1 BOTTLE (63629-3868-4)Jul 26, 2011
63629-3868-560 TABLET, FILM COATED in 1 BOTTLE (63629-3868-5)Dec 14, 2010
63629-3868-610 TABLET, FILM COATED in 1 BOTTLE (63629-3868-6)Dec 3, 2013
63629-3868-790 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7)Mar 6, 2023

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