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Tramadal Hydrochloride and Acetaminophen - 49349-791-03 - (Tramadal Hydrochloride and Acetaminophen)

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Drug Information of Tramadal Hydrochloride and Acetaminophen

Product NDC: 49349-791
Proprietary Name: Tramadal Hydrochloride and Acetaminophen
Non Proprietary Name: Tramadal Hydrochloride and Acetaminophen
Active Ingredient(s): 325; 37.5    mg/1; mg/1 & nbsp;   Tramadal Hydrochloride and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tramadal Hydrochloride and Acetaminophen

Product NDC: 49349-791
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077858
Marketing Category: ANDA
Start Marketing Date: 20111017

Package Information of Tramadal Hydrochloride and Acetaminophen

Package NDC: 49349-791-03
Package Description: 20 TABLET in 1 BLISTER PACK (49349-791-03)

NDC Information of Tramadal Hydrochloride and Acetaminophen

NDC Code 49349-791-03
Proprietary Name Tramadal Hydrochloride and Acetaminophen
Package Description 20 TABLET in 1 BLISTER PACK (49349-791-03)
Product NDC 49349-791
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadal Hydrochloride and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111017
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE
Strength Number 325; 37.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Tramadal Hydrochloride and Acetaminophen


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