Home NDC 0002-7669 CYRAMZA
Product NDC 0002-7669
11-digit product format 000027669
Labeler code 0002
Product ID 0002-7669_161cb5e7-7955-45e5-bdde-9be94fdbe76a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ramucirumab
Dosage form SOLUTION
Route INTRAVENOUS
Labeler Eli Lilly and Company
Application BLA125477
Marketing category BLA
Marketing start 2014-04-21
Substance RAMUCIRUMAB
Active strength 10 mg/mL
Pharmacologic classes VEGFR2 Inhibitors [MoA], Vascular Endothelial Growth Factor Receptor 2 Antagonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base CYRAMZA
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RAMUCIRUMAB 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination D99YVK4L0X Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 4 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1657775 Internal RxNorm lookup 1657777 Internal RxNorm lookup 1657780 Internal RxNorm lookup 1657781 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0002-7669-01 CYRAMZA 1 in 1 CARTON SOLUTION 1 47 0002-7669-01 CYRAMZA 10 mL in 1 VIAL, SINGLE-DOSE SOLUTION 10 47
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0002-7669 CYRAMZA (RAMUCIRUMAB) SOLUTION [ELI LILLY AND COMPANY] 45 Current NDC, Legacy NDC, 2 package rows 20250418_c6080942-dee6-423e-b688-1272c2ae90d4.zip
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 · 1 matching rows.
Purple Book Biologic Products# BLA, Proprietary name, Proper name table BLA Proprietary name Proper name License type Status Latest source 125477 Cyramza ramucirumab 351(a) Rx 2026-09-01
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0002-7669-01 00002766901 1 VIAL, SINGLE-DOSE in 1 CARTON (0002-7669-01) / 10 mL in 1 VIAL, SINGLE-DOSE 2014-04-21 0000-00-00 No No Current