Home NDC 16590-266 NDC 16590-266 - CLONIDINE 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 16590-266
Package NDCs from labels 16590-266-30, 16590-266-60, 16590-266-71, 16590-266-72, 16590-266-90
Manufacturer STAT RX USA LLC
Effective date 2010-03-15
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type CLONIDINE - STAT RX USA LLC STAT RX USA LLC 2010-03-15 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 16590-266-30 CLONIDINE 30 in 1 BOTTLE, PLASTIC TABLET 30 2 16590-266-60 CLONIDINE 60 in 1 BOTTLE, PLASTIC TABLET 60 2 16590-266-71 CLONIDINE 100 in 1 BOTTLE, PLASTIC TABLET 100 2 16590-266-72 CLONIDINE 120 in 1 BOTTLE, PLASTIC TABLET 120 2 16590-266-90 CLONIDINE 90 in 1 BOTTLE, PLASTIC TABLET 90 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 16590-266 CLONIDINE (CLONIDINE HCL) TABLET [STAT RX USA LLC] 2 5 package rows 20100401_438dece9-95d4-40f2-84b4-9e2c6d88e760.zip
DailyMed Socrata Ingredients#