NDC 72189-323 – Ciprofloxacin

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

Human Prescription Drug

Product NDC72189-323

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Direct Rx
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
February 21, 2022
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
72189-323-066 TABLET, COATED in 1 BOTTLE (72189-323-06)Feb 21, 2022

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