Home NDC 59556-118 NDC 59556-118 - IBUPROFEN 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 59556-118
Package NDCs from labels 59556-118-01, 59556-118-02
Manufacturer Strides Pharma Inc
Effective date 2023-04-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type IBUPROFEN - Strides Pharma Inc Strides Pharma Inc 2023-04-07 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59556-118-01 IBUPROFEN 15 mL in 1 BOTTLE, DROPPER SUSPENSION 15 2 59556-118-01 IBUPROFEN 1 in 1 CARTON SUSPENSION 1 2 59556-118-02 IBUPROFEN 1 in 1 CARTON SUSPENSION 1 2 59556-118-02 IBUPROFEN 30 mL in 1 BOTTLE, DROPPER SUSPENSION 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59556-118 IBUPROFEN SUSPENSION [STRIDES PHARMA INC] 2 4 package rows 20250406_7101b241-0e0d-4bdf-b9fd-3d0970ebd14e.zip