49726-041 NDC - SYNAPTOL ()

Drug Information

  • Product NDC: 49726-041
  • Proprietary Name: Synaptol
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: HelloLife, Inc.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/11/2017
End Marketing Date:7/1/2024

Package Information

No. Package Code Package Description Billing Unit
149726-041-6060 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (49726-041-60)

NDC Record

Field Name Field Value Definition
PRODUCT NDC49726-041The 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 NAMESynaptolThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/11/2017The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
END MARKETING DATE7/1/2024The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICThe translation of the dosage form Code submitted by the firm.
LABELER NAMEHelloLife, Inc.The translation of the route code submitted by the firm, indicating route of administration.

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

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