NDC 69238-2432 – Ciprofloxacin

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

Human Prescription Drug

Product NDC69238-2432

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075939
Marketed since
February 29, 2024
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
69238-2432-1100 TABLET, FILM COATED in 1 BOTTLE (69238-2432-1)Feb 29, 2024

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