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Tramadol Hydrochloride - 65162-627-10 - (Tramadol Hydrochloride)

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Drug Information of Tramadol Hydrochloride

Product NDC: 65162-627
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tramadol Hydrochloride

Product NDC: 65162-627
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076003
Marketing Category: ANDA
Start Marketing Date: 20101115

Package Information of Tramadol Hydrochloride

Package NDC: 65162-627-10
Package Description: 100 TABLET, COATED in 1 BOTTLE (65162-627-10)

NDC Information of Tramadol Hydrochloride

NDC Code 65162-627-10
Proprietary Name Tramadol Hydrochloride
Package Description 100 TABLET, COATED in 1 BOTTLE (65162-627-10)
Product NDC 65162-627
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tramadol Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20101115
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
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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