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oxycodone hydrochloride - 58177-681-04 - (oxycodone hydrochloride)

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Drug Information of oxycodone hydrochloride

Product NDC: 58177-681
Proprietary Name: oxycodone hydrochloride
Non Proprietary Name: oxycodone hydrochloride
Active Ingredient(s): 40    mg/1 & nbsp;   oxycodone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of oxycodone hydrochloride

Product NDC: 58177-681
Labeler Name: Ethex Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020553
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20090925

Package Information of oxycodone hydrochloride

Package NDC: 58177-681-04
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (58177-681-04)

NDC Information of oxycodone hydrochloride

NDC Code 58177-681-04
Proprietary Name oxycodone hydrochloride
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (58177-681-04)
Product NDC 58177-681
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090925
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Ethex Corporation
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of oxycodone hydrochloride


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