Home NDC 68083-359-01 NDC 68083-359-01 - Doxercalciferol 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 68083-359
Requested NDC 68083-359-01
Package NDCs from labels 68083-359-01, 68083-359-50
Manufacturer Gland Pharma Limited
Effective date 2024-11-06
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 68083-359-01 Doxercalciferol 2 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 2 6 68083-359-50 Doxercalciferol 50 in 1 CARTON INJECTION, SOLUTION 50 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68083-359 DOXERCALCIFEROL INJECTION, SOLUTION [GLAND PHARMA LIMITED] 6 Current NDC, 2 package rows 20241107_f0d79a1b-c7fb-4521-941a-5d6c2fd50170.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 125 of 186 · 3,705 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.