OxyContin - 60760-049-90 - (oxycodone hydrochloride)

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Drug Information of OxyContin

Product NDC: 60760-049
Proprietary Name: OxyContin
Non Proprietary Name: oxycodone hydrochloride
Active Ingredient(s): 20    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 OxyContin

Product NDC: 60760-049
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020553
Marketing Category: NDA
Start Marketing Date: 20101230

Package Information of OxyContin

Package NDC: 60760-049-90
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60760-049-90)

NDC Information of OxyContin

NDC Code 60760-049-90
Proprietary Name OxyContin
Package Description 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60760-049-90)
Product NDC 60760-049
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 20101230
Marketing Category Name NDA
Labeler Name St Marys Medical Park Pharmacy
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OxyContin


General Information