NDC 69238-2434 – Ciprofloxacin

Ciprofloxacin Hydrochloride 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC69238-2434

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 (2)

Package NDCDescriptionSince
69238-2434-1100 TABLET, FILM COATED in 1 BOTTLE (69238-2434-1)Feb 29, 2024
69238-2434-550 TABLET, FILM COATED in 1 BOTTLE (69238-2434-5)Feb 29, 2024

Other Ciprofloxacin products