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pdf |
pdfManufacturer Name
NDC1
NDC2
NDC3 Alternate ID Alternate ID Website URL
Brand Name Generic Name
Volume Per Item
Unit for Volume per Item
Number of Items Per
NDC or Alternate ID
Package Type Strength Unit for Strength
FDA Application
Number / Registration
Number
FDA Application
Supplement Number
Additional FDA
Application Number #1
Additional FDA
Application Supplement
Number #1
Additional FDA
Application Number #2
Additional FDA
Application Supplement
Number #2
FDA Approval Date
FDA Approval Type
First Marketing Date
Date of First Sale for this
Product
File Type | application/pdf |
File Title | Template |
Author | Michelle Berman |
File Modified | 2024-01-24 |
File Created | 2024-01-24 |