FDA.reportPublic FDA data

AMINOPENTAMIDE SULFATE

Manufacturer
PROFESSIONAL GROUP OF PHARMACISTS NEW YORK LLC
Effective date
2022-01-01
Label type
BULK INGREDIENT
Version
2
Source
full-release
Hydrated at
2026-06-01 02:50:20

Label at a glance#

ProductAMINOPENTAMIDE SULFATE
Active ingredientAMINOPENTAMIDE SULFATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

aminopentamidelabel.jpgPACKAGE LABEL IMAGEPACKAGE LABEL IMAGE

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72969-00272969-002-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOPENTAMIDE SULFATE20P9NI883OACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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