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OXYCODONE HYDROCHLORIDE - 43063-220-90 - (oxycodone hydrochloride)

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Drug Information of OXYCODONE HYDROCHLORIDE

Product NDC: 43063-220
Proprietary Name: OXYCODONE HYDROCHLORIDE
Non Proprietary Name: oxycodone hydrochloride
Active Ingredient(s): 30    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: 43063-220
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077712
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of OXYCODONE HYDROCHLORIDE

Package NDC: 43063-220-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-220-90)

NDC Information of OXYCODONE HYDROCHLORIDE

NDC Code 43063-220-90
Proprietary Name OXYCODONE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-220-90)
Product NDC 43063-220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OXYCODONE HYDROCHLORIDE


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