FDA.reportPublic FDA data

NDC 58181-5200 - Sevoflurane

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
58181-5200
Package NDCs from labels
58181-5200-1
Manufacturer
NextSource Pharma | Shandong New Time Pharmaceutical Co., Ltd.
Effective date
2024-08-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sevoflurane USPNextSource Pharma | Shandong New Time Pharmaceutical Co., Ltd.2024-08-09HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58181-5200-1Sevoflurane250 mL in 1 BOTTLE, GLASSLIQUID2505
58181-5200-1Sevoflurane1 in 1 PACKAGELIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58181-5200SEVOFLURANE LIQUID [NEXTSOURCE PHARMA]52 package rows20240810_fbcdf809-e968-418b-af21-477e1fa0cee6.zip