NDC 0143-9928 – Ciprofloxacin

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

Human Prescription Drug 1 recall

Product NDC0143-9928

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076558
Marketed since
June 9, 2004
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (3)

Package NDCDescriptionSince
0143-9928-01100 TABLET, FILM COATED in 1 BOTTLE (0143-9928-01)Jun 9, 2004
0143-9928-05500 TABLET, FILM COATED in 1 BOTTLE (0143-9928-05)Jun 9, 2004
0143-9928-3030 TABLET, FILM COATED in 1 BOTTLE (0143-9928-30)Jun 9, 2004

Recalls mentioning this NDC

Other ciprofloxacin products