Tramapap - 64038-059-03 - (Tramadol Hydrochloride, Acetaminophen)

Alphabetical Index


Drug Information of Tramapap

Product NDC: 64038-059
Proprietary Name: Tramapap
Non Proprietary Name: Tramadol Hydrochloride, Acetaminophen
Active Ingredient(s):    & nbsp;   Tramadol Hydrochloride, Acetaminophen
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Tramapap

Product NDC: 64038-059
Labeler Name: Living Well Pharmacy, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100407

Package Information of Tramapap

Package NDC: 64038-059-03
Package Description: 1 KIT in 1 KIT (64038-059-03) * 15 g in 1 BOTTLE (64038-738-15) * 75 g in 1 BOTTLE (64038-135-75)

NDC Information of Tramapap

NDC Code 64038-059-03
Proprietary Name Tramapap
Package Description 1 KIT in 1 KIT (64038-059-03) * 15 g in 1 BOTTLE (64038-738-15) * 75 g in 1 BOTTLE (64038-135-75)
Product NDC 64038-059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride, Acetaminophen
Dosage Form Name KIT
Route Name
Start Marketing Date 20100407
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Living Well Pharmacy, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Tramapap


General Information