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Tramadol Hydrochloride - 51079-991-56 - (tramadol hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 51079-991
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: 51079-991
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075986
Marketing Category: ANDA
Start Marketing Date: 20000903

Package Information of Tramadol Hydrochloride

Package NDC: 51079-991-56
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-991-56) > 30 TABLET, FILM COATED in 1 BLISTER PACK (51079-991-30)

NDC Information of Tramadol Hydrochloride

NDC Code 51079-991-56
Proprietary Name Tramadol Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-991-56) > 30 TABLET, FILM COATED in 1 BLISTER PACK (51079-991-30)
Product NDC 51079-991
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000903
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
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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