NDC 71205-997 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71205-997

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076126
Marketed since
October 10, 2009
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (6)

Package NDCDescriptionSince
71205-997-00100 TABLET, FILM COATED in 1 BOTTLE (71205-997-00)Mar 25, 2020
71205-997-1010 TABLET, FILM COATED in 1 BOTTLE (71205-997-10)Mar 25, 2020
71205-997-1414 TABLET, FILM COATED in 1 BOTTLE (71205-997-14)Mar 25, 2020
71205-997-2020 TABLET, FILM COATED in 1 BOTTLE (71205-997-20)Mar 25, 2020
71205-997-3030 TABLET, FILM COATED in 1 BOTTLE (71205-997-30)Mar 25, 2020
71205-997-55500 TABLET, FILM COATED in 1 BOTTLE (71205-997-55)Mar 25, 2020

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