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  4. NDC Product Code: 64038-059 Tramapap

NDC 64038-059 Tramapap

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64038-059?
  4. Tramapap Uses
  5. Active Ingredients UNII Codes
  6. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
64038-059
Proprietary Name:
Tramapap
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Living Well Pharmacy, Inc.
Labeler Code:
64038
Product Label ID:
e142844d-a0f3-4b33-a3ca-795456bafa1a
Start Marketing Date: [9]
04-07-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64038-059-03

Package Description: 1 KIT in 1 KIT * 75 g in 1 BOTTLE (64038-135-75) * 15 g in 1 BOTTLE (64038-738-15)

Product Details

What is NDC 64038-059?

The NDC code 64038-059 is assigned by the FDA to the product Tramapap which is product labeled by Living Well Pharmacy, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64038-059-03 1 kit in 1 kit * 75 g in 1 bottle (64038-135-75) * 15 g in 1 bottle (64038-738-15). 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 Tramapap?

EquipmentRequired supplies needed to compound this kitEquipment ItemQuantityTramadol HCl (Included)15 gramsAcetaminophen (Included)75 gramsLactose Monohydrate Spray Dried Powder ( Included)23.25 gramsRiboflavin Powder (Included)1.5 gramsRed/Blue #1 Capsules ( Required Not Included)300 Capsules

Which are Tramapap UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Tramapap?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 999729 - traMADol HCl 50 MG / acetaminophen 250 MG Oral Capsule
  • RxCUI: 999729 - acetaminophen 250 MG / tramadol hydrochloride 50 MG Oral Capsule
  • RxCUI: 999729 - APAP 250 MG / tramadol hydrochloride 50 MG Oral Capsule

* 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".