NDC 71335-1152 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71335-1152

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin Tablets
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
July 13, 2019
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1152-07 TABLET, COATED in 1 BOTTLE (71335-1152-0)Jan 29, 2025
71335-1152-120 TABLET, COATED in 1 BOTTLE (71335-1152-1)Jan 29, 2025
71335-1152-210 TABLET, COATED in 1 BOTTLE (71335-1152-2)Jan 29, 2025
71335-1152-314 TABLET, COATED in 1 BOTTLE (71335-1152-3)Jan 29, 2025
71335-1152-46 TABLET, COATED in 1 BOTTLE (71335-1152-4)Jan 29, 2025
71335-1152-530 TABLET, COATED in 1 BOTTLE (71335-1152-5)Jan 29, 2025
71335-1152-660 TABLET, COATED in 1 BOTTLE (71335-1152-6)Jan 29, 2025
71335-1152-712 TABLET, COATED in 1 BOTTLE (71335-1152-7)Jan 29, 2025
71335-1152-840 TABLET, COATED in 1 BOTTLE (71335-1152-8)Jan 29, 2025
71335-1152-990 TABLET, COATED in 1 BOTTLE (71335-1152-9)Jan 29, 2025

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