59746-284 NDC - PANTOPRAZOLE SODIUM

Drug Information

  • Product NDC: 59746-284
  • Proprietary Name:
  • Non Proprietary Name: Pantoprazole Sodium
  • Active Ingredient(s): 40 mg/1 PANTOPRAZOLE SODIUM
  • Administration Route(s):
  • Dosage Form(s): TABLET, DELAYED RELEASE

Labeler Information

Field Name Field Value
Labeler Name: JUBILANT CADISTA PHARMACEUTICALS INC.
Product Type: DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category: DRUG FOR FURTHER PROCESSING
Start Marketing Date:9/1/2011
End Marketing Date:12/1/2021

Package Information

No. Package Code Package Description Billing Unit
159746-284-01100 TABLET, DELAYED RELEASE in 1 BOTTLE (59746-284-01)
259746-284-0310 BLISTER PACK in 1 CARTON (59746-284-03) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
359746-284-05500 TABLET, DELAYED RELEASE in 1 BOTTLE (59746-284-05)
459746-284-101000 TABLET, DELAYED RELEASE in 1 BOTTLE (59746-284-10)
559746-284-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (59746-284-30)
659746-284-711 BAG in 1 DRUM (59746-284-71) / 1 BAG in 1 BAG / 25000 TABLET, DELAYED RELEASE in 1 BAG
759746-284-9090 TABLET, DELAYED RELEASE in 1 BOTTLE (59746-284-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC59746-284The 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 DATE9/1/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct 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.
LABELER NAMEJubilant Cadista Pharmacuticals Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC59746-284The 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 DATE9/1/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEDRUG FOR FURTHER PROCESSINGProduct 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.
LABELER NAMEJUBILANT CADISTA 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: 12/19/2025

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