54973-3354 NDC - MENOPAUSE PLUS ENERGY ()

Drug Information

  • Product NDC: 54973-3354
  • Proprietary Name: Menopause Plus Energy
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Hyland's Inc.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/1/2018
End Marketing Date:10/15/2025

Package Information

No. Package Code Package Description Billing Unit
154973-3354-11 KIT in 1 CARTON (54973-3354-1) * 4 TABLET in 1 PACKET (54973-3353-2) * 60 TABLET in 1 BOTTLE, PLASTIC (54973-3353-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC54973-3354The 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 NAMEMenopause Plus EnergyIndicates 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 DATE6/1/2018The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
END MARKETING DATE10/15/2025The 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 NAMEHyland's Inc.This is the date that the labeler indicates was the start of its marketing of the drug product.

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

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