Home NDC 11695-7034 NDC 11695-7034 - ACEPROMAZINE MALEATE 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 11695-7034
Package NDCs from labels 11695-7034-1, 11695-7034-2
Manufacturer Covetrus North America | ZYVET ANIMAL HEALTH INC.
Effective date 2024-11-08
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 11695-7034-1 ACEPROMAZINE MALEATE 100 in 1 BOTTLE TABLET 100 1 11695-7034-2 ACEPROMAZINE MALEATE 500 in 1 BOTTLE TABLET 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11695-7034 ACEPROMAZINE MALEATE TABLET [COVETRUS NORTH AMERICA] 1 2 package rows 20241116_934fcdff-5ae4-48f5-baa0-ddf549662a56.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.