NDC 65862-077 – Ciprofloxacin

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

Human Prescription Drug

Product NDC65862-077

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
April 26, 2007
Marketing end
February 28, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (2)

Package NDCDescriptionSince
65862-077-01100 TABLET, FILM COATED in 1 BOTTLE (65862-077-01)Apr 26, 2007
65862-077-05500 TABLET, FILM COATED in 1 BOTTLE (65862-077-05)Apr 26, 2007

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