NDC 16571-412 – ciprofloxacin

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

Human Prescription Drug 1 recall

Product NDC16571-412

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 (2)

Package NDCDescriptionSince
16571-412-10100 TABLET, FILM COATED in 1 BOTTLE (16571-412-10)Sep 10, 2004
16571-412-50500 TABLET, FILM COATED in 1 BOTTLE (16571-412-50)Sep 10, 2004

Recalls mentioning this NDC

Other ciprofloxacin products