FDA.reportPublic FDA data

NDC 72969-022 - METAMIZOLE SODIUM

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
72969-022
Package NDCs from labels
72969-022-10
Manufacturer
PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
Effective date
2019-03-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
METAMIZOLE SODIUM - PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLCPROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC2019-03-14BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72969-022-10METAMIZOLE SODIUM1 g in 1 PACKAGEPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72969-022METAMIZOLE SODIUM POWDER [PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC]11 package rows20210307_883f2214-e3f5-4877-8429-1223a66e58f2.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.