NDC 76420-045 – Ciprofloxacin

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

Human Prescription Drug

Product NDC76420-045

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
April 26, 2007
Marketing end
October 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (5)

Package NDCDescriptionSince
76420-045-066 TABLET, FILM COATED in 1 BOTTLE (76420-045-06)Sep 4, 2020
76420-045-1010 TABLET, FILM COATED in 1 BOTTLE (76420-045-10)Sep 4, 2020
76420-045-1414 TABLET, FILM COATED in 1 BOTTLE (76420-045-14)Sep 4, 2020
76420-045-2020 TABLET, FILM COATED in 1 BOTTLE (76420-045-20)Sep 4, 2020
76420-045-3030 TABLET, FILM COATED in 1 BOTTLE (76420-045-30)Sep 4, 2020

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