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Oxycodone Hydrochloride - 54868-3137-3 - (oxycodone hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 54868-3137
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: oxycodone hydrochloride
Active Ingredient(s): 10    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: 54868-3137
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077290
Marketing Category: ANDA
Start Marketing Date: 20080606

Package Information of Oxycodone Hydrochloride

Package NDC: 54868-3137-3
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (54868-3137-3)

NDC Information of Oxycodone Hydrochloride

NDC Code 54868-3137-3
Proprietary Name Oxycodone Hydrochloride
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (54868-3137-3)
Product NDC 54868-3137
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080606
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


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