NDC 71335-2097 – Ciprofloxacin

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

Human Prescription Drug

Product NDC71335-2097

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
August 12, 2020
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2097-07 TABLET, COATED in 1 BOTTLE (71335-2097-0)Apr 3, 2024
71335-2097-120 TABLET, COATED in 1 BOTTLE (71335-2097-1)Jun 24, 2022
71335-2097-210 TABLET, COATED in 1 BOTTLE (71335-2097-2)Jul 5, 2022
71335-2097-314 TABLET, COATED in 1 BOTTLE (71335-2097-3)Jul 22, 2022
71335-2097-46 TABLET, COATED in 1 BOTTLE (71335-2097-4)Oct 28, 2022
71335-2097-530 TABLET, COATED in 1 BOTTLE (71335-2097-5)Apr 3, 2024
71335-2097-660 TABLET, COATED in 1 BOTTLE (71335-2097-6)Apr 3, 2024
71335-2097-712 TABLET, COATED in 1 BOTTLE (71335-2097-7)Apr 3, 2024
71335-2097-840 TABLET, COATED in 1 BOTTLE (71335-2097-8)Apr 3, 2024
71335-2097-990 TABLET, COATED in 1 BOTTLE (71335-2097-9)Apr 3, 2024

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