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TRAMADOL HYDROCHLORIDE - 47335-533-18 - (TRAMADOL HYDROCHLORIDE)

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Drug Information of TRAMADOL HYDROCHLORIDE

Product NDC: 47335-533
Proprietary Name: TRAMADOL HYDROCHLORIDE
Non Proprietary Name: TRAMADOL HYDROCHLORIDE
Active Ingredient(s): 200    mg/1 & nbsp;   TRAMADOL HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of TRAMADOL HYDROCHLORIDE

Product NDC: 47335-533
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091607
Marketing Category: ANDA
Start Marketing Date: 20111230

Package Information of TRAMADOL HYDROCHLORIDE

Package NDC: 47335-533-18
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-18)

NDC Information of TRAMADOL HYDROCHLORIDE

NDC Code 47335-533-18
Proprietary Name TRAMADOL HYDROCHLORIDE
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-18)
Product NDC 47335-533
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111230
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of TRAMADOL HYDROCHLORIDE


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