Home NDC 48106-1151-2 NDC 48106-1151-2 - StepSept PB-50 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 48106-1151
Requested NDC 48106-1151-2
Package NDCs from labels 48106-1151-1, 48106-1151-2, 48106-1151-3, 48106-1151-4, 48106-1151-5, 48106-1151-6
Manufacturer BouMatic, LLC | Knapp Manufacturing
Effective date 2012-01-01
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 48106-1151-1 StepSept PB-50 3.8 L in 1 DRUM LIQUID 3.8 2 48106-1151-2 StepSept PB-50 18.9 L in 1 DRUM LIQUID 18.9 2 48106-1151-3 StepSept PB-50 56.8 L in 1 DRUM LIQUID 56.8 2 48106-1151-4 StepSept PB-50 114 L in 1 DRUM LIQUID 114 2 48106-1151-5 StepSept PB-50 208 L in 1 DRUM LIQUID 208 2 48106-1151-6 StepSept PB-50 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK LIQUID 1040 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48106-1151 STEPSEPT PB-50 (LAURAMINE OXIDE) LIQUID [BOUMATIC, LLC] 2 6 package rows 20120530_60f32ab8-eeb6-46ce-b301-93f6061e5b0b.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.