NDC 83939-0002 – Ciprofloxacin Hydrochloride

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

Human Prescription Drug

Product NDC83939-0002

Product details

Brand name
Ciprofloxacin Hydrochloride
Generic name
Ciprofloxacin Hydrochloride
Labeler
VERITYRX, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076593
Marketed since
May 23, 2024
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
83939-0002-11 TABLET, FILM COATED in 1 POUCH (83939-0002-1)Nov 3, 2025
83939-0002-250 POUCH in 1 BOX, UNIT-DOSE (83939-0002-2) / 1 TABLET, FILM COATED in 1 POUCHNov 3, 2025
83939-0002-3100 POUCH in 1 BOX, UNIT-DOSE (83939-0002-3) / 1 TABLET, FILM COATED in 1 POUCHNov 3, 2025

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