NDC 58657-675 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC58657-675

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Method Pharmaceuticals, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
August 12, 2020
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
58657-675-01100 TABLET, COATED in 1 BOTTLE (58657-675-01)Aug 12, 2020

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