Home NDC 63629-8699-01 NDC 63629-8699-01 - Podocon 25 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 63629-8699
Requested NDC 63629-8699-01
Package NDCs from labels 63629-8699-1, 63629-8699-01
Manufacturer Bryant Ranch Prepack
Effective date 2023-07-17
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Podocon 25 - Bryant Ranch Prepack Bryant Ranch Prepack 2023-07-17 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63629-8699-1 Podocon 25 1 in 1 CARTON TINCTURE 1 103 63629-8699-1 Podocon 25 15 mL in 1 BOTTLE, WITH APPLICATOR TINCTURE 15 103
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63629-8699 PODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [BRYANT RANCH PREPACK] 103 Current NDC, Legacy NDC, 2 package rows 20230718_a13345b7-c42b-4459-b0ff-03cf91e46b7d.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 6 of 141 · 2,805 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.