Home NDC 55529-155-04 NDC 55529-155-04 - Norfenicol 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 55529-155
Requested NDC 55529-155-04
Package NDCs from labels 55529-155-02, 55529-155-04, 55529-155-05
Manufacturer Norbrook Laboratories Limited
Effective date 2022-02-01
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 55529-155-02 Norfenicol 1 in 1 CARTON INJECTION, SOLUTION 1 3 55529-155-02 Norfenicol 100 mL in 1 BOTTLE, PLASTIC INJECTION, SOLUTION 100 3 55529-155-04 Norfenicol 250 mL in 1 BOTTLE, PLASTIC INJECTION, SOLUTION 250 3 55529-155-05 Norfenicol 500 mL in 1 BOTTLE, PLASTIC INJECTION, SOLUTION 500 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55529-155 NORFENICOL (FLORFENICOL) INJECTION, SOLUTION [NORBROOK LABORATORIES LIMITED] 3 4 package rows 20220204_ece3cea4-7011-4c0e-9d4a-4e8c14486da7.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.