NDC 53157-129 Leukotrap

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
Proprietary Name:
Product Type: [3]
Labeler Name: [5]
Haemonetics Manufacturing Inc
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Structure:
Code Navigator:

Product Packages

NDC Code 53157-129-63

Package Description: 18 BAG in 1 CARTON / 1 KIT in 1 BAG * 70 mL in 1 BAG * 110 mL in 1 BAG

Product Details

What is NDC 53157-129?

The NDC code 53157-129 is assigned by the FDA to the product Leukotrap which is product labeled by Haemonetics Manufacturing Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53157-129-63 18 bag in 1 carton / 1 kit in 1 bag * 70 ml in 1 bag * 110 ml in 1 bag. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Leukotrap?

Instructions for Use for Systems Containing a Y Sampling Site (YSS) with or without a pre-attached Vacuum Tube Holder or Sample Diversion Pouch (SDP) with a pre-attached Vacuum Tube Holder. See unit foil envelope for specific product code/description being used.Figure 1- Diagram of the Complete Product Set

Which are Leukotrap UNII Codes?

The UNII codes for the active ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".