Home NDC 48664-001-01 NDC 48664-001-01 - Oxygen 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 48664-001
Requested NDC 48664-001-01
Package NDCs from labels 48664-001-01, 48664-001-02
Manufacturer Weiler Welding Company
Effective date 2016-11-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Oxygen - Weiler Welding Company Weiler Welding Company 2016-11-07 HUMAN PRESCRIPTION DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48664-001-01 Oxygen 154344 L in 1 CYLINDER LIQUID 154344 9 48664-001-02 Oxygen 1 in 1 CYLINDER LIQUID 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48664-001 OXYGEN LIQUID [WEILER WELDING COMPANY] 9 Legacy NDC, 2 package rows 20161108_712afac5-3ad9-4bb3-88e0-ffa1b17e6553.zip
DailyMed Socrata Ingredients# 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 23 of 28 · 552 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.