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oxycodone hydrochloride - 60505-3539-1 - (oxycodone hydrochloride)

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Drug Information of oxycodone hydrochloride

Product NDC: 60505-3539
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, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of oxycodone hydrochloride

Product NDC: 60505-3539
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020553
Marketing Category: NDA
Start Marketing Date: 19951201

Package Information of oxycodone hydrochloride

Package NDC: 60505-3539-1
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3539-1)

NDC Information of oxycodone hydrochloride

NDC Code 60505-3539-1
Proprietary Name oxycodone hydrochloride
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3539-1)
Product NDC 60505-3539
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19951201
Marketing Category Name NDA
Labeler Name Apotex Corp.
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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