NDC 50090-1648 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-1648

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
A-S Medication Solutions
Dosage form
Tablet
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 (7)

Package NDCDescriptionSince
50090-1648-020 TABLET in 1 BOTTLE (50090-1648-0)Jan 19, 2015
50090-1648-114 TABLET in 1 BOTTLE (50090-1648-1)Jan 19, 2015
50090-1648-36 TABLET in 1 BOTTLE (50090-1648-3)Jan 19, 2015
50090-1648-428 TABLET in 1 BOTTLE (50090-1648-4)Jan 19, 2015
50090-1648-510 TABLET in 1 BOTTLE (50090-1648-5)Jan 19, 2015
50090-1648-730 TABLET in 1 BOTTLE (50090-1648-7)Jan 19, 2015
50090-1648-81 TABLET in 1 BOTTLE (50090-1648-8)May 22, 2018

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