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Tramadol Hydrochloride - 55289-719-98 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 55289-719
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: 55289-719
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076003
Marketing Category: ANDA
Start Marketing Date: 20091123

Package Information of Tramadol Hydrochloride

Package NDC: 55289-719-98
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (55289-719-98)

NDC Information of Tramadol Hydrochloride

NDC Code 55289-719-98
Proprietary Name Tramadol Hydrochloride
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (55289-719-98)
Product NDC 55289-719
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 PD-Rx 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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