Home NDC 0091-3371 NDC 0091-3371 - FLUXID 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 0091-3371
Package NDCs from labels 0091-3371-32, 0091-3371-01
Manufacturer Schwarz Pharma
Effective date 2006-11-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type FLUXID - Schwarz Pharma Schwarz Pharma 2006-11-07 Human prescription drug label
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0091-3371-01 FLUXID 100 in 1 BOTTLE TABLET, ORALLY DISINTEGRATING 100 2 0091-3371-32 FLUXID 30 in 1 BOTTLE TABLET, ORALLY DISINTEGRATING 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0091-3371 FLUXID (FAMOTIDINE) TABLET, ORALLY DISINTEGRATING [SCHWARZ PHARMA] 2 Unmatched 20061201_ADB54FE50FCC4A01AFC64AA3D3DB45BB.zip