62559-713 NDC - DESIPRAMINE HYDROCHLORIDE ()

Drug Information

  • Product NDC: 62559-713
  • Proprietary Name: Desipramine Hydrochloride
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: ANI Pharmaceuticals, Inc.
Product Type:
FDA Application Number: ANDA205153
Marketing Category: ANDA
Start Marketing Date:1/22/2019
End Marketing Date:12/31/2020

Package Information

No. Package Code Package Description Billing Unit
162559-713-01100 TABLET, FILM COATED in 1 BOTTLE (62559-713-01)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC62559-713The 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 NAMEDesipramine HydrochlorideIndicates 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 DATE1/22/2019The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
END MARKETING DATE12/31/2020The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAMEANDAThe translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBERANDA205153This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEANI Pharmaceuticals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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

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