24236-296 NDC - TRIHEXYPHENIDYL HYDROCHLORIDE ()

Drug Information

  • Product NDC: 24236-296
  • Proprietary Name: Trihexyphenidyl Hydrochloride
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: REMEDYREPACK INC.
Product Type:
FDA Application Number: ANDA040337
Marketing Category: ANDA
Start Marketing Date:3/27/2013
End Marketing Date:3/27/2014

Package Information

No. Package Code Package Description Billing Unit
124236-296-20100 TABLET in 1 CANISTER (24236-296-20)

NDC Record

Field Name Field Value Definition
PRODUCT NDC24236-296The 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 NAMETrihexyphenidyl HydrochlorideThe 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.
START MARKETING DATE3/27/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE3/27/2014The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEANDAThe translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBERANDA040337This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEREMEDYREPACK INC.Product 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.

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This page was last updated on: 3/6/2026

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