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TRAMADOL HYDROCHLORIDE - 68382-319-10 - (TRAMADOL HYDROCHLORIDE)

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Drug Information of TRAMADOL HYDROCHLORIDE

Product NDC: 68382-319
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TRAMADOL HYDROCHLORIDE

Product NDC: 68382-319
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090404
Marketing Category: ANDA
Start Marketing Date: 20110131

Package Information of TRAMADOL HYDROCHLORIDE

Package NDC: 68382-319-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (68382-319-10)

NDC Information of TRAMADOL HYDROCHLORIDE

NDC Code 68382-319-10
Proprietary Name TRAMADOL HYDROCHLORIDE
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (68382-319-10)
Product NDC 68382-319
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAMADOL HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110131
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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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