Home NDC 49553-1261-2 NDC 49553-1261-2 - Ceftiofur Free Acid 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 49553-1261
Requested NDC 49553-1261-2
Package NDCs from labels 49553-1261-1, 49553-1261-2
Manufacturer Qilu SYNVA Pharmaceutical Co., Ltd.
Effective date 2026-01-21
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 49553-1261-1 Ceftiofur Free Acid 3 kg in 1 TANK POWDER 3 3 49553-1261-2 Ceftiofur Free Acid 5 kg in 1 TANK POWDER 5 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49553-1261 CEFTIOFUR FREE ACID POWDER [QILU SYNVA PHARMACEUTICAL CO., LTD.] 2 2 package rows 20211023_4bac37a1-541c-4aa0-bd7d-89f3b431d360.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.