62037-605 NDC - LORATADINE AND PSEUDOEPHEDRINE SULFATE

Drug Information

  • Product NDC: 62037-605
  • Proprietary Name:
  • Non Proprietary Name: Loratadine and Pseudoephedrine Sulfate
  • Active Ingredient(s): 10 mg/1 LORATADINE; 240 mg/1 PSEUDOEPHEDRINE SULFATE
  • Administration Route(s):
  • Dosage Form(s): TABLET, EXTENDED RELEASE

Labeler Information

Field Name Field Value
Labeler Name: Actavis Pharma, Inc.
Product Type: DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category: DRUG FOR FURTHER PROCESSING
Start Marketing Date:2/21/2003

Package Information

No. Package Code Package Description Billing Unit
162037-605-0810638 TABLET, EXTENDED RELEASE in 1 BOX (62037-605-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62037-605An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
PRODUCT TYPE NAMEDRUG FOR FURTHER PROCESSINGIndicates 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 NAMELoratadine and Pseudoephedrine Sulfate 
DOSAGE FORM NAMETABLET, EXTENDED RELEASEThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE2/21/2003This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEDRUG FOR FURTHER PROCESSINGThis is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
LABELER NAMEActavis Pharma, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMELORATADINE; PSEUDOEPHEDRINE SULFATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10; 240 
ACTIVE INGRED UNITmg/1; mg/1 

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

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