Home NDC 53002-2008 NDC 53002-2008 - Enalapril 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 53002-2008
Package NDCs from labels 53002-2008-0, 53002-2008-3
Manufacturer RPK Pharmaceuticals, Inc.
Effective date 2023-01-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Rx only RPK Pharmaceuticals, Inc. 2023-01-31 HUMAN PRESCRIPTION DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53002-2008-0 Enalapril maleate 100 in 1 BOTTLE TABLET 100 2 53002-2008-3 Enalapril maleate 30 in 1 BOTTLE TABLET 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53002-2008 ENALAPRIL MALEATE TABLET [RPK PHARMACEUTICALS, INC.] 2 2 package rows 20230602_03e9a8d7-1aa3-4eec-b22c-0596cd1bb883.zip