NDC 0615-8630 – Ciprofloxacin

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

Human Prescription Drug

Product NDC0615-8630

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Hydrochloride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077859
Marketed since
March 27, 2025
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (3)

Package NDCDescriptionSince
0615-8630-1010 TABLET, FILM COATED in 1 BLISTER PACK (0615-8630-10)Apr 13, 2026
0615-8630-1414 TABLET, FILM COATED in 1 BLISTER PACK (0615-8630-14)Apr 13, 2026
0615-8630-2020 TABLET, FILM COATED in 1 BLISTER PACK (0615-8630-20)Apr 13, 2026

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