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Tramadol Hydrochloride - 55154-6239-3 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 55154-6239
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tramadol Hydrochloride

Product NDC: 55154-6239
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075986
Marketing Category: ANDA
Start Marketing Date: 20020621

Package Information of Tramadol Hydrochloride

Package NDC: 55154-6239-3
Package Description: 6 BLISTER PACK in 1 CARTON (55154-6239-3) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Tramadol Hydrochloride

NDC Code 55154-6239-3
Proprietary Name Tramadol Hydrochloride
Package Description 6 BLISTER PACK in 1 CARTON (55154-6239-3) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-6239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020621
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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