NDC 71335-2502 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2502

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
October 1, 2023
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
71335-2502-07 TABLET in 1 BOTTLE (71335-2502-0)Sep 23, 2024
71335-2502-120 TABLET in 1 BOTTLE (71335-2502-1)Sep 23, 2024
71335-2502-210 TABLET in 1 BOTTLE (71335-2502-2)Sep 23, 2024
71335-2502-314 TABLET in 1 BOTTLE (71335-2502-3)Sep 23, 2024
71335-2502-46 TABLET in 1 BOTTLE (71335-2502-4)Sep 23, 2024
71335-2502-530 TABLET in 1 BOTTLE (71335-2502-5)Sep 23, 2024
71335-2502-660 TABLET in 1 BOTTLE (71335-2502-6)Sep 23, 2024
71335-2502-712 TABLET in 1 BOTTLE (71335-2502-7)Sep 23, 2024
71335-2502-840 TABLET in 1 BOTTLE (71335-2502-8)Sep 23, 2024
71335-2502-990 TABLET in 1 BOTTLE (71335-2502-9)Sep 23, 2024

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