Home NDC 61133-4010-1 NDC 61133-4010-1 - Macrosyn 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 61133-4010
Requested NDC 61133-4010-1
Package NDCs from labels 61133-4010-2, 61133-4010-1, 61133-4010-3, 61133-4010-4
Manufacturer Bimeda, Inc. | Bimeda- MTC
Effective date 2024-10-30
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 61133-4010-1 Macrosyn 50 mL in 1 VIAL, GLASS INJECTION, SOLUTION 50 3 61133-4010-2 Macrosyn 100 mL in 1 VIAL, GLASS INJECTION, SOLUTION 100 3 61133-4010-3 Macrosyn 250 mL in 1 VIAL, GLASS INJECTION, SOLUTION 250 3 61133-4010-4 Macrosyn 500 mL in 1 VIAL, GLASS INJECTION, SOLUTION 500 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61133-4010 MACROSYN (TULATHROMYCIN) INJECTION, SOLUTION [BIMEDA, INC.] 3 4 package rows 20241101_5d1e9d53-5b39-4f17-a9a6-c9fa5bbd23fe.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.