NDC 59651-873 – Ciprofloxacin

Ciprofloxacin Hydrochloride 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC59651-873

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
February 9, 2024
Marketing end
February 29, 2028
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
59651-873-5050 TABLET, FILM COATED in 1 BOTTLE (59651-873-50)Feb 9, 2024

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