FDA.reportPublic FDA data

NDC 72835-100-00 - Protezall

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
72835-100
Requested NDC
72835-100-00
Package NDCs from labels
72835-100-00
Manufacturer
V2 Pharma
Effective date
2023-06-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Protezall - V2 PharmaV2 Pharma2023-06-27MEDICAL DEVICE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72835-100-00Protezall4 in 1 BOX43
72835-100-00Protezall1 in 1 POUCH13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72835-100PROTEZALL () [V2 PHARMA]32 package rows20230628_28118063-81cf-48a8-b886-848fb349dfb3.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72835-100-00EA - Each72835-1006a249268-5f95-4015-bca6-5510cd2c126512023-06-06

Reported adverse events (FAERS/openFDA)#

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