47133-575 NDC - ELEPSIA XR ()

Drug Information

  • Product NDC: 47133-575
  • Proprietary Name: Elepsia XR
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Sun Pharma Advanced Research Company Limited
Product Type:
FDA Application Number: NDA204417
Marketing Category: NDA
Start Marketing Date:5/17/2019

Package Information

No. Package Code Package Description Billing Unit
147133-575-13500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47133-575-13)
247133-575-8330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47133-575-83)
347133-575-88100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47133-575-88)

NDC Record

Field Name Field Value Definition
PRODUCT NDC47133-575The 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 NAMEElepsia XRThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/17/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct 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.
APPLICATION NUMBERNDA204417This 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 NAMESun Pharma Advanced Research Company LimitedName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/4/2025

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