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Tramadol Hydrochloride - 0093-0058-01 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 0093-0058
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: 0093-0058
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075977
Marketing Category: ANDA
Start Marketing Date: 20020620

Package Information of Tramadol Hydrochloride

Package NDC: 0093-0058-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-0058-01)

NDC Information of Tramadol Hydrochloride

NDC Code 0093-0058-01
Proprietary Name Tramadol Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-0058-01)
Product NDC 0093-0058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020620
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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