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TRAMADOL HYDROCHLORIDE - 47335-859-08 - (TRAMADOL HYDROCHLORIDE)

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Drug Information of TRAMADOL HYDROCHLORIDE

Product NDC: 47335-859
Proprietary Name: TRAMADOL HYDROCHLORIDE
Non Proprietary Name: TRAMADOL HYDROCHLORIDE
Active Ingredient(s): 100    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: 47335-859
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201384
Marketing Category: ANDA
Start Marketing Date: 20111212

Package Information of TRAMADOL HYDROCHLORIDE

Package NDC: 47335-859-08
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-08)

NDC Information of TRAMADOL HYDROCHLORIDE

NDC Code 47335-859-08
Proprietary Name TRAMADOL HYDROCHLORIDE
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-08)
Product NDC 47335-859
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111212
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of TRAMADOL HYDROCHLORIDE


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