NDC 63629-1010 – Ciprofloxacin

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

Human Prescription Drug

Product NDC63629-1010

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076126
Marketed since
October 10, 2009
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (8)

Package NDCDescriptionSince
63629-1010-1100 TABLET, FILM COATED in 1 BOTTLE (63629-1010-1)Dec 7, 2020
63629-1010-220 TABLET, FILM COATED in 1 BOTTLE (63629-1010-2)Sep 23, 2020
63629-1010-330 TABLET, FILM COATED in 1 BOTTLE (63629-1010-3)Apr 6, 2022
63629-1010-414 TABLET, FILM COATED in 1 BOTTLE (63629-1010-4)Oct 25, 2021
63629-1010-5500 TABLET, FILM COATED in 1 BOTTLE (63629-1010-5)Nov 17, 2020
63629-1010-660 TABLET, FILM COATED in 1 BOTTLE (63629-1010-6)Apr 6, 2022
63629-1010-710 TABLET, FILM COATED in 1 BOTTLE (63629-1010-7)Apr 6, 2022
63629-1010-8120 TABLET, FILM COATED in 1 BOTTLE (63629-1010-8)Apr 6, 2022

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