83532-001 NDC - GANODERMA LUCIDUM SPORES POLYSACCHARIDES ()

Drug Information

  • Product NDC: 83532-001
  • Proprietary Name: GANODERMA LUCIDUM SPORES POLYSACCHARIDES
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Bestway Biomedical Technology (Shanghai) Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:6/17/2023
End Marketing Date:6/18/2023

Package Information

No. Package Code Package Description Billing Unit
183532-001-01300 CAPSULE in 1 BOX (83532-001-01)
283532-001-0130 CAPSULE in 1 BOX (83532-001-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83532-001The 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 NAMEGANODERMA LUCIDUM SPORES POLYSACCHARIDESThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/17/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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 NAMEBestway Biomedical Technology (Shanghai) Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC83532-001The 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 NAMEGANODERMA LUCIDUM SPORES POLYSACCHARIDESThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/17/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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 NAMEBestway Biomedical Technology (Shanghai) Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025