NDC 71610-159 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71610-159

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
April 26, 2007
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
71610-159-833600 TABLET, FILM COATED in 1 BOTTLE (71610-159-83)Sep 20, 2018

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