NDC 76420-214 – Ciprofloxacin

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

Human Prescription Drug

Product NDC76420-214

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076558
Marketed since
June 9, 2004
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (5)

Package NDCDescriptionSince
76420-214-066 TABLET, FILM COATED in 1 BOTTLE (76420-214-06)Mar 8, 2022
76420-214-1010 TABLET, FILM COATED in 1 BOTTLE (76420-214-10)Mar 8, 2022
76420-214-1414 TABLET, FILM COATED in 1 BOTTLE (76420-214-14)Mar 8, 2022
76420-214-2020 TABLET, FILM COATED in 1 BOTTLE (76420-214-20)Mar 8, 2022
76420-214-3030 TABLET, FILM COATED in 1 BOTTLE (76420-214-30)Mar 8, 2022

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