Home DailyMed 5cd35e38-b820-4309-ab72-b2111c769b4c TIROFIBAN HYDROCHLORIDE INJECTION Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Amdipharm Limited
Effective date 2022-03-28
Label type Bulk Ingredient
Version 2
Source full-release
Hydrated at 2026-06-01 02:50:25 Label at a glance# Product Tirofiban Hydrochloride
Active ingredient TIROFIBAN HYDROCHLORIDE
Label structure 1 sections
DailyMed Pharmacologic Classes# DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82169-025-50 Tirofiban Hydrochloride 48 in 1 CASE INJECTION 48 2 82169-025-50 Tirofiban Hydrochloride 50 mL in 1 VIAL, GLASS INJECTION 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82169-025 TIROFIBAN HYDROCHLORIDE INJECTION [AMDIPHARM LIMITED] 2 2 package rows 20220330_5cd35e38-b820-4309-ab72-b2111c769b4c.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 6 matching rows.
Tirofiban Hydrochloride TIROFIBAN ANHYDROUS CITRIC ACID TRISODIUM CITRATE DIHYDRATE SODIUM CHLORIDE WATER Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 5 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 3 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.