NDC 68788-8200 – Ciprofloxacin

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

Human Prescription Drug

Product NDC68788-8200

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
May 24, 2022
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
68788-8200-110 TABLET, COATED in 1 BOTTLE (68788-8200-1)May 24, 2022
68788-8200-220 TABLET, COATED in 1 BOTTLE (68788-8200-2)May 24, 2022
68788-8200-330 TABLET, COATED in 1 BOTTLE (68788-8200-3)May 24, 2022

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