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OXYCODONE HYDROCHLORIDE - 10702-057-01 - (oxycodone hydrochloride)

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Drug Information of OXYCODONE HYDROCHLORIDE

Product NDC: 10702-057
Proprietary Name: OXYCODONE HYDROCHLORIDE
Non Proprietary Name: oxycodone hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   oxycodone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of OXYCODONE HYDROCHLORIDE

Product NDC: 10702-057
Labeler Name: KVK-TECH, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091393
Marketing Category: ANDA
Start Marketing Date: 20091012

Package Information of OXYCODONE HYDROCHLORIDE

Package NDC: 10702-057-01
Package Description: 100 TABLET in 1 BOTTLE (10702-057-01)

NDC Information of OXYCODONE HYDROCHLORIDE

NDC Code 10702-057-01
Proprietary Name OXYCODONE HYDROCHLORIDE
Package Description 100 TABLET in 1 BOTTLE (10702-057-01)
Product NDC 10702-057
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091012
Marketing Category Name ANDA
Labeler Name KVK-TECH, INC.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OXYCODONE HYDROCHLORIDE


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