NDC 72189-111 – Ciprofloxacin

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

Human Prescription Drug

Product NDC72189-111

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin hydrochloride
Labeler
DIRECT RX
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
June 12, 2020
Marketing end
February 28, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (4)

Package NDCDescriptionSince
72189-111-1010 TABLET, FILM COATED in 1 BOTTLE (72189-111-10)Jun 12, 2020
72189-111-1414 TABLET, FILM COATED in 1 BOTTLE (72189-111-14)Jun 12, 2020
72189-111-2020 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)Jun 12, 2020
72189-111-3030 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)Jun 12, 2020

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