67467-182 NDC - WILATE - VON WILLEBRAND FACTOR/COAGULATION FACTOR VIII COMPLEX (HUMAN) ()

Drug Information

  • Product NDC: 67467-182
  • Proprietary Name: Wilate - von Willebrand Factor/Coagulation Factor VIII Complex (Human)
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
Product Type:
FDA Application Number: BLA125251
Marketing Category: BLA
Start Marketing Date:12/4/2009

Package Information

No. Package Code Package Description Billing Unit
167467-182-015 mL in 1 VIAL (67467-182-01)EA
267467-182-0210 mL in 1 VIAL (67467-182-02)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC67467-182The 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 NAMEWilate - von Willebrand Factor/Coagulation Factor VIII Complex (Human)The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/4/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEBLAProduct 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 NUMBERBLA125251This 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 NAMEOctapharma Pharmazeutika Produktionsgesellschaft m.b.H.Name of Company corresponding to the labeler code segment of the Product NDC.

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

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