NDC 62135-309 – Ciprofloxacin

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

Human Prescription Drug

Product NDC62135-309

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin hydrochloride
Labeler
Chartwell RX, LLC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076896
Marketed since
April 13, 2021
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (5)

Package NDCDescriptionSince
62135-309-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-309-01)Apr 13, 2021
62135-309-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-309-05)Apr 13, 2021
62135-309-101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-309-10)Apr 13, 2021
62135-309-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-309-20)Apr 13, 2021
62135-309-2828 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-309-28)Apr 13, 2021

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