NDC 51655-216 – Ciprofloxacin

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

Human Prescription Drug

Product NDC51655-216

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
March 17, 2023
Marketing end
February 28, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (6)

Package NDCDescriptionSince
51655-216-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-20)Jun 28, 2023
51655-216-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-25)Aug 18, 2023
51655-216-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-52)Jan 10, 2024
51655-216-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-53)Jul 14, 2023
51655-216-8414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-84)Jun 8, 2023
51655-216-876 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-87)Mar 17, 2023

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