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Tramadol Hydrochloride - 10544-531-15 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 10544-531
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: 10544-531
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076003
Marketing Category: ANDA
Start Marketing Date: 20100407

Package Information of Tramadol Hydrochloride

Package NDC: 10544-531-15
Package Description: 15 TABLET in 1 BOTTLE (10544-531-15)

NDC Information of Tramadol Hydrochloride

NDC Code 10544-531-15
Proprietary Name Tramadol Hydrochloride
Package Description 15 TABLET in 1 BOTTLE (10544-531-15)
Product NDC 10544-531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100407
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, 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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