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Tramadol Hydrochloride - 35356-659-20 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 35356-659
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: 35356-659
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076003
Marketing Category: ANDA
Start Marketing Date: 20091123

Package Information of Tramadol Hydrochloride

Package NDC: 35356-659-20
Package Description: 20 TABLET in 1 BOTTLE (35356-659-20)

NDC Information of Tramadol Hydrochloride

NDC Code 35356-659-20
Proprietary Name Tramadol Hydrochloride
Package Description 20 TABLET in 1 BOTTLE (35356-659-20)
Product NDC 35356-659
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091123
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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