Home NDC 49553-4661-2 NDC 49553-4661-2 - Flunixin Meglumine This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 49553-4661
Requested NDC 49553-4661-2
Package NDCs from labels 49553-4661-1, 49553-4661-2
Manufacturer Qilu SYNVA Pharmaceutical Co., Ltd.
Effective date 2026-08-19
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49553-4661-1 Flunixin Meglumine 25 kg in 1 DRUM POWDER 25 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49553-4661 FLUNIXIN MEGLUMINE POWDER [QILU SYNVA PHARMACEUTICAL CO., LTD.] 6 1 package rows 20211218_e2ae81cf-3fa7-4757-b3f9-0a781ad40031.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.