NDC 68788-0985 Tramadol Hydrochloride And Acetaminophen

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:
68788-0985
Proprietary Name:
Tramadol Hydrochloride And Acetaminophen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Preferred Pharmaceuticals, Inc.
Labeler Code:
68788
Start Marketing Date: [9]
12-17-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 68788-0985-1

Package Description: 100 TABLET in 1 BOTTLE, DISPENSING

NDC Code 68788-0985-2

Package Description: 20 TABLET in 1 BOTTLE, DISPENSING

NDC Code 68788-0985-3

Package Description: 30 TABLET in 1 BOTTLE, DISPENSING

NDC Code 68788-0985-4

Package Description: 40 TABLET in 1 BOTTLE, DISPENSING

NDC Code 68788-0985-5

Package Description: 50 TABLET in 1 BOTTLE, DISPENSING

NDC Code 68788-0985-6

Package Description: 60 TABLET in 1 BOTTLE, DISPENSING

NDC Code 68788-0985-8

Package Description: 120 TABLET in 1 BOTTLE, DISPENSING

NDC Code 68788-0985-9

Package Description: 90 TABLET in 1 BOTTLE, DISPENSING

Product Details

What is NDC 68788-0985?

The NDC code 68788-0985 is assigned by the FDA to the product Tramadol Hydrochloride And Acetaminophen which is product labeled by Preferred Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 68788-0985-1 100 tablet in 1 bottle, dispensing , 68788-0985-2 20 tablet in 1 bottle, dispensing , 68788-0985-3 30 tablet in 1 bottle, dispensing , 68788-0985-4 40 tablet in 1 bottle, dispensing , 68788-0985-5 50 tablet in 1 bottle, dispensing , 68788-0985-6 60 tablet in 1 bottle, dispensing , 68788-0985-8 120 tablet in 1 bottle, dispensing , 68788-0985-9 90 tablet in 1 bottle, dispensing . 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 is the NDC to RxNorm Crosswalk for Tramadol Hydrochloride And Acetaminophen?

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: 836395 - traMADol HCl 37.5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 836395 - acetaminophen 325 MG / tramadol hydrochloride 37.5 MG Oral Tablet
  • RxCUI: 836395 - APAP 325 MG / tramadol hydrochloride 37.5 MG Oral Tablet

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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".