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Oxycodone Hydrochloride - 13107-055-99 - (Oxycodone Hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 13107-055
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 5    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: 13107-055
Labeler Name: Aurolife Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202160
Marketing Category: ANDA
Start Marketing Date: 20120712

Package Information of Oxycodone Hydrochloride

Package NDC: 13107-055-99
Package Description: 1000 TABLET in 1 BOTTLE (13107-055-99)

NDC Information of Oxycodone Hydrochloride

NDC Code 13107-055-99
Proprietary Name Oxycodone Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (13107-055-99)
Product NDC 13107-055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120712
Marketing Category Name ANDA
Labeler Name Aurolife Pharma LLC
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


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