Home NDC 0061-1116 NDC 0061-1116 - Nuflor 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 0061-1116
Package NDCs from labels 0061-1116-04, 0061-1116-05, 0061-1116-06
Manufacturer Merck Sharp & Dohme Corp.
Effective date 2024-11-15
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 0061-1116-04 Nuflor 1 in 1 CARTON INJECTION, SOLUTION 1 5 0061-1116-04 Nuflor 100 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 100 5 0061-1116-05 Nuflor 250 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 250 5 0061-1116-05 Nuflor 1 in 1 CARTON INJECTION, SOLUTION 1 5 0061-1116-06 Nuflor 500 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 500 5 0061-1116-06 Nuflor 1 in 1 CARTON INJECTION, SOLUTION 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0061-1116 NUFLOR (FLORFENICOL) INJECTION, SOLUTION [MERCK SHARP & DOHME CORP.] 5 6 package rows 20241116_87f37539-b83b-42e9-989c-32e63ebecd29.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.