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oxycodone hydrochloride - 63629-4155-2 - (oxycodone hydrochloride)

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Drug Information of oxycodone hydrochloride

Product NDC: 63629-4155
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of oxycodone hydrochloride

Product NDC: 63629-4155
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077712
Marketing Category: ANDA
Start Marketing Date: 20100308

Package Information of oxycodone hydrochloride

Package NDC: 63629-4155-2
Package Description: 60 CAPSULE in 1 BOTTLE (63629-4155-2)

NDC Information of oxycodone hydrochloride

NDC Code 63629-4155-2
Proprietary Name oxycodone hydrochloride
Package Description 60 CAPSULE in 1 BOTTLE (63629-4155-2)
Product NDC 63629-4155
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100308
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
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


General Information