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TRAMADOL HYDROCHLORIDE - 52125-317-03 - (TRAMADOL HYDROCHLORIDE)

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Drug Information of TRAMADOL HYDROCHLORIDE

Product NDC: 52125-317
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: 52125-317
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021692
Marketing Category: NDA
Start Marketing Date: 20130508

Package Information of TRAMADOL HYDROCHLORIDE

Package NDC: 52125-317-03
Package Description: 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-317-03)

NDC Information of TRAMADOL HYDROCHLORIDE

NDC Code 52125-317-03
Proprietary Name TRAMADOL HYDROCHLORIDE
Package Description 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-317-03)
Product NDC 52125-317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130508
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
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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