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Tramadol Hydrochloride - 42858-901-03 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 42858-901
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: 42858-901
Labeler Name: Rhodes Pharmaceuticals L.P.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021745
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111230

Package Information of Tramadol Hydrochloride

Package NDC: 42858-901-03
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42858-901-03)

NDC Information of Tramadol Hydrochloride

NDC Code 42858-901-03
Proprietary Name Tramadol Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42858-901-03)
Product NDC 42858-901
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 NDA AUTHORIZED GENERIC
Labeler Name Rhodes Pharmaceuticals L.P.
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


General Information