NDC 0143-9927 – Ciprofloxacin

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

Human Prescription Drug 1 recall

Product NDC0143-9927

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
0143-9927-01100 TABLET, FILM COATED in 1 BOTTLE (0143-9927-01)Jun 9, 2004
0143-9927-05500 TABLET, FILM COATED in 1 BOTTLE (0143-9927-05)Jun 9, 2004
0143-9927-3030 TABLET, FILM COATED in 1 BOTTLE (0143-9927-30)Jun 9, 2004

Recalls mentioning this NDC

Other Ciprofloxacin products