Home NDC 17856-0948 NDC 17856-0948 - Potassium Chloride 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 17856-0948
Package NDCs from labels 17856-0948-3, 17856-0948-1, 17856-0948-4, 17856-0948-2
Manufacturer ATLANTIC BIOLOGICALS CORP.
Effective date 2024-01-02
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 17856-0948-1 Potassium Chloride 72 in 1 BOX, UNIT-DOSE SOLUTION 72 2 17856-0948-2 Potassium Chloride 50 in 1 BOX, UNIT-DOSE SOLUTION 50 2 17856-0948-3 Potassium Chloride 15 mL in 1 CUP, UNIT-DOSE SOLUTION 15 2 17856-0948-4 Potassium Chloride 30 mL in 1 CUP, UNIT-DOSE SOLUTION 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17856-0948 POTASSIUM CHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORP.] 2 4 package rows 20240103_3037feb3-5d7b-4be4-84af-5e29aa0e9d08.zip