50370-0023 NDC - TOLTERODINE TARTRATE

Drug Information

Product NDC: 50370-0023
Proprietary Name:
Non Proprietary Name: Tolterodine Tartrate
Active Ingredient(s): 1 kg/kg TOLTERODINE TARTRATE
Administration Route(s):
Dosage Form(s): POWDER

Labeler Information

Field Name	Field Value
Labeler Name:	MSN Pharmachem Private Limited
Product Type:	BULK INGREDIENT
FDA Application Number:
Marketing Category:	BULK INGREDIENT
Start Marketing Date:	4/20/2010

Package Information

No.	Package Code	Package Description	Billing Unit
1	50370-0023-1	60 kg in 1 DRUM (50370-0023-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	50370-0023	The 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.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates 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.
NON PROPRIETARY NAME	Tolterodine Tartrate	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
DOSAGE FORM NAME	POWDER	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
START MARKETING DATE	4/20/2010	The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAME	BULK INGREDIENT	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	MSN Pharmachem Private Limited	This is the date that the labeler indicates was the start of its marketing of the drug product.
SUBSTANCE NAME	TOLTERODINE TARTRATE	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.
ACTIVE NUMERATOR STRENGTH	1	This 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.
ACTIVE INGRED UNIT	kg/kg	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/7/2026

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