NDC 68788-8136 – Ciprofloxacin

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

Human Prescription Drug

Product NDC68788-8136

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
February 3, 2022
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8136-06 TABLET, FILM COATED in 1 BOTTLE (68788-8136-0)Feb 3, 2022
68788-8136-114 TABLET, FILM COATED in 1 BOTTLE (68788-8136-1)Feb 3, 2022
68788-8136-220 TABLET, FILM COATED in 1 BOTTLE (68788-8136-2)Feb 3, 2022
68788-8136-330 TABLET, FILM COATED in 1 BOTTLE (68788-8136-3)Feb 3, 2022
68788-8136-810 TABLET, FILM COATED in 1 BOTTLE (68788-8136-8)Feb 3, 2022

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