NDC 16571-411 – Ciprofloxacin

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

Human Prescription Drug 1 recall

Product NDC16571-411

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
September 10, 2004
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
16571-411-10100 TABLET, FILM COATED in 1 BOTTLE (16571-411-10)Sep 10, 2004

Recalls mentioning this NDC

Other Ciprofloxacin products