Home NDC 48106-1200-2 NDC 48106-1200-2 - HC-PRE 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 48106-1200
Requested NDC 48106-1200-2
Package NDCs from labels 48106-1200-2, 48106-1200-1
Manufacturer BouMatic, LLC
Effective date 2013-07-01
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type HC-PRE - BouMatic, LLC BouMatic, LLC 2013-07-01 OTC ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48106-1200-1 HC-PRE 18.9 L in 1 DRUM LIQUID 18.9 2 48106-1200-2 HC-PRE 56.8 L in 1 DRUM LIQUID 56.8 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48106-1200 HC-PRE (PRE-DIP ADDITIVE) LIQUID [BOUMATIC, LLC] 2 2 package rows 20140401_caea5afe-8124-4a5d-8a2d-4030b6d95934.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.