NDC 72969-002 - AMINOPENTAMIDE SULFATE

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
72969-002
Package NDCs from labels
72969-002-10
Manufacturer
PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
Effective date
2022-01-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AMINOPENTAMIDE SULFATE - PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLCPROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC2022-01-01BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72969-002-10AMINOPENTAMIDE SULFATE1 g in 1 PACKAGEPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72969-002AMINOPENTAMIDE SULFATE POWDER [PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC]21 package rows20220114_a02f0e00-94ff-4ccf-a57d-a8d9012af03f.zip