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TRAMADOL HYDROCHLORIDE - 60505-0171-8 - (TRAMADOL HYDROCHLORIDE)

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Drug Information of TRAMADOL HYDROCHLORIDE

Product NDC: 60505-0171
Proprietary Name: TRAMADOL HYDROCHLORIDE
Non Proprietary Name: TRAMADOL HYDROCHLORIDE
Active Ingredient(s): 50    mg/1 & nbsp;   TRAMADOL HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TRAMADOL HYDROCHLORIDE

Product NDC: 60505-0171
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075981
Marketing Category: ANDA
Start Marketing Date: 20020710

Package Information of TRAMADOL HYDROCHLORIDE

Package NDC: 60505-0171-8
Package Description: 1000 TABLET, COATED in 1 BOTTLE (60505-0171-8)

NDC Information of TRAMADOL HYDROCHLORIDE

NDC Code 60505-0171-8
Proprietary Name TRAMADOL HYDROCHLORIDE
Package Description 1000 TABLET, COATED in 1 BOTTLE (60505-0171-8)
Product NDC 60505-0171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20020710
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of TRAMADOL HYDROCHLORIDE


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