NDC 51655-490 – Ciprofloxacin

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

Human Prescription Drug

Product NDC51655-490

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
January 5, 2023
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (5)

Package NDCDescriptionSince
51655-490-2020 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-20)Feb 3, 2023
51655-490-5230 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-52)Jan 5, 2023
51655-490-5310 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-53)Feb 3, 2023
51655-490-8414 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-84)Jan 20, 2023
51655-490-876 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-87)Jan 5, 2023

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