Home NDC 83335-101 NDC 83335-101 - CuraTUSSIN 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 83335-101
Package NDCs from labels 83335-101-16, 83335-101-08, 83335-101-04
Manufacturer Wittman Pharma, Inc.
Effective date 2024-04-18
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type CuraTUSSIN Wittman Pharma, Inc. 2024-04-18 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83335-101-04 CuraTUSSIN 118 mL in 1 BOTTLE, PLASTIC SOLUTION 118 4 83335-101-08 CuraTUSSIN 237 mL in 1 BOTTLE, PLASTIC SOLUTION 237 4 83335-101-16 CuraTUSSIN 473 mL in 1 BOTTLE, PLASTIC SOLUTION 473 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83335-101 CURATUSSIN (GUAIFENESIN) SOLUTION [WITTMAN PHARMA, INC.] 4 3 package rows 20240420_0fc8ab3f-23d8-ce01-e063-6394a90aab0f.zip