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TRAMADOL HYDROCHLORIDE - 49884-823-11 - (tramadol hydrochloride)

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Drug Information of TRAMADOL HYDROCHLORIDE

Product NDC: 49884-823
Proprietary Name: TRAMADOL HYDROCHLORIDE
Non Proprietary Name: tramadol hydrochloride
Active Ingredient(s): 300    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: 49884-823
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078783
Marketing Category: ANDA
Start Marketing Date: 20110921

Package Information of TRAMADOL HYDROCHLORIDE

Package NDC: 49884-823-11
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-823-11)

NDC Information of TRAMADOL HYDROCHLORIDE

NDC Code 49884-823-11
Proprietary Name TRAMADOL HYDROCHLORIDE
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-823-11)
Product NDC 49884-823
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110921
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name TRAMADOL HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of TRAMADOL HYDROCHLORIDE


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