NDC 61442-223 – Ciprofloxacin

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

Human Prescription Drug

Product NDC61442-223

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Carlsbad Technology, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076126
Marketed since
October 10, 2009
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
61442-223-01100 TABLET, FILM COATED in 1 BOTTLE (61442-223-01)Oct 10, 2009
61442-223-05500 TABLET, FILM COATED in 1 BOTTLE (61442-223-05)Oct 10, 2009

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