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tramadol hydrochloride - 63629-2868-4 - (tramadol hydrochloride)

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Drug Information of tramadol hydrochloride

Product NDC: 63629-2868
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
Coding System: National Drug Codes(NDC)

Labeler Information of tramadol hydrochloride

Product NDC: 63629-2868
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075964
Marketing Category: ANDA
Start Marketing Date: 20020622

Package Information of tramadol hydrochloride

Package NDC: 63629-2868-4
Package Description: 100 TABLET in 1 BOTTLE (63629-2868-4)

NDC Information of tramadol hydrochloride

NDC Code 63629-2868-4
Proprietary Name tramadol hydrochloride
Package Description 100 TABLET in 1 BOTTLE (63629-2868-4)
Product NDC 63629-2868
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tramadol hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020622
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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