43742-1032 NDC - VER ()

Drug Information

  • Product NDC: 43742-1032
  • Proprietary Name: Ver
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/22/2017
End Marketing Date:12/2/2022

Package Information

No. Package Code Package Description Billing Unit
143742-1032-160 mL in 1 BOTTLE, DROPPER (43742-1032-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1032The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEVerIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE6/22/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE12/2/2022The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICThe translation of the route code submitted by the firm, indicating route of administration.
LABELER NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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