58264-0007 NDC - D7 ()

Drug Information

  • Product NDC: 58264-0007
  • Proprietary Name: D7
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: DNA Labs, Inc.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/1/1990

Package Information

No. Package Code Package Description Billing Unit
158264-0007-129.57 mL in 1 BOTTLE, GLASS (58264-0007-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC58264-0007The 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 NAMED7The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/1990This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEDNA Labs, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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

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