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Tramadol Hydrochloride - 0378-4151-01 - (tramadol hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 0378-4151
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: 0378-4151
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075986
Marketing Category: ANDA
Start Marketing Date: 20111027

Package Information of Tramadol Hydrochloride

Package NDC: 0378-4151-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4151-01)

NDC Information of Tramadol Hydrochloride

NDC Code 0378-4151-01
Proprietary Name Tramadol Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4151-01)
Product NDC 0378-4151
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111027
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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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