NDC 59651-978 – Ciprofloxacin

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

Human Prescription Drug

Product NDC59651-978

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 (5)

Package NDCDescriptionSince
59651-978-01100 TABLET, FILM COATED in 1 BOTTLE (59651-978-01)Mar 27, 2025
59651-978-05500 TABLET, FILM COATED in 1 BOTTLE (59651-978-05)Mar 27, 2025
59651-978-2020 TABLET, FILM COATED in 1 BOTTLE (59651-978-20)Mar 27, 2025
59651-978-5050 TABLET, FILM COATED in 1 BOTTLE (59651-978-50)Mar 27, 2025
59651-978-981000 TABLET, FILM COATED in 1 BOTTLE (59651-978-98)Mar 27, 2025

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