NDC 51407-775 – Ciprofloxacin

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

Human Prescription Drug

Product NDC51407-775

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076126
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 (1)

Package NDCDescriptionSince
51407-775-01100 TABLET, FILM COATED in 1 BOTTLE (51407-775-01)May 7, 2024

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