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  4. NDC Product Code: 62007-309 Pcxx Snf Rns Bubblegum

NDC 62007-309 Pcxx Snf Rns Bubblegum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 62007-309?
  5. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
62007-309
Proprietary Name:
Pcxx Snf Rns Bubblegum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ross Healthcare Inc.
Labeler Code:
62007
Product Label ID:
8b10d964-448f-4053-e053-2995a90a1d72
Start Marketing Date: [9]
06-11-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
BUBBLE GUM (C73368)

Product Packages

NDC Code 62007-309-64

Package Description: 1900 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 62007-309?

The NDC code 62007-309 is assigned by the FDA to the product Pcxx Snf Rns Bubblegum which is product labeled by Ross Healthcare Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62007-309-64 1900 ml in 1 bottle, plastic . 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.

Which are Pcxx Snf Rns Bubblegum 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".