NDC 68788-4177 – Ciprofloxacin Hydrochloride

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

Human Prescription Drug

Product NDC68788-4177

Product details

Brand name
Ciprofloxacin Hydrochloride
Generic name
Ciprofloxacin Hydrochloride
Labeler
Preferred Pharmaceuticals Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076593
Marketed since
July 31, 2026
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
68788-4177-06 TABLET, FILM COATED in 1 BOTTLE (68788-4177-0)Jul 31, 2026
68788-4177-114 TABLET, FILM COATED in 1 BOTTLE (68788-4177-1)Jul 31, 2026
68788-4177-220 TABLET, FILM COATED in 1 BOTTLE (68788-4177-2)Jul 31, 2026
68788-4177-330 TABLET, FILM COATED in 1 BOTTLE (68788-4177-3)Jul 31, 2026
68788-4177-810 TABLET, FILM COATED in 1 BOTTLE (68788-4177-8)Jul 31, 2026

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