NDC 71205-636 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71205-636

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
April 26, 2007
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (7)

Package NDCDescriptionSince
71205-636-066 TABLET, FILM COATED in 1 BOTTLE (71205-636-06)Feb 2, 2022
71205-636-1010 TABLET, FILM COATED in 1 BOTTLE (71205-636-10)Feb 2, 2022
71205-636-1414 TABLET, FILM COATED in 1 BOTTLE (71205-636-14)Feb 3, 2022
71205-636-2020 TABLET, FILM COATED in 1 BOTTLE (71205-636-20)Feb 2, 2022
71205-636-3030 TABLET, FILM COATED in 1 BOTTLE (71205-636-30)Feb 2, 2022
71205-636-6060 TABLET, FILM COATED in 1 BOTTLE (71205-636-60)Feb 2, 2022
71205-636-9090 TABLET, FILM COATED in 1 BOTTLE (71205-636-90)Feb 2, 2022

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