NDC 59651-976 – Ciprofloxacin

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

Human Prescription Drug

Product NDC59651-976

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
March 27, 2025
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (4)

Package NDCDescriptionSince
59651-976-01100 TABLET, FILM COATED in 1 BOTTLE (59651-976-01)Mar 27, 2025
59651-976-2020 TABLET, FILM COATED in 1 BOTTLE (59651-976-20)Mar 27, 2025
59651-976-3030 TABLET, FILM COATED in 1 BOTTLE (59651-976-30)Mar 27, 2025
59651-976-991000 TABLET, FILM COATED in 1 BOTTLE (59651-976-99)Mar 27, 2025

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