NDC 62135-308 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC62135-308

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 (3)

Package NDCDescriptionSince
62135-308-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-308-01)Apr 13, 2021
62135-308-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-308-20)Apr 13, 2021
62135-308-2828 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62135-308-28)Apr 13, 2021

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