0091-3324 NDC - NIRAVAM ()

Drug Information

  • Product NDC: 0091-3324
  • Proprietary Name: Niravam
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: UCB, Inc.
Product Type:
FDA Application Number: NDA021726
Marketing Category: NDA
Start Marketing Date:1/20/2005
End Marketing Date:5/31/2013

Package Information

No. Package Code Package Description Billing Unit
10091-3324-01100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0091-3324-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0091-3324The 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 NAMENiravamIndicates 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 DATE1/20/2005The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
END MARKETING DATE5/31/2013The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMENDAThe translation of the dosage form Code submitted by the firm.
APPLICATION NUMBERNDA021726The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAMEUCB, Inc.This is the date that the labeler indicates was the start of its marketing of the drug product.

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This page was last updated on: 12/19/2025