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OXYCODONE HYDROCHLORIDE - 10544-599-02 - (oxycodone hydrochloride)

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Drug Information of OXYCODONE HYDROCHLORIDE

Product NDC: 10544-599
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: 10544-599
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076758
Marketing Category: ANDA
Start Marketing Date: 20100406

Package Information of OXYCODONE HYDROCHLORIDE

Package NDC: 10544-599-02
Package Description: 120 TABLET in 1 BOTTLE (10544-599-02)

NDC Information of OXYCODONE HYDROCHLORIDE

NDC Code 10544-599-02
Proprietary Name OXYCODONE HYDROCHLORIDE
Package Description 120 TABLET in 1 BOTTLE (10544-599-02)
Product NDC 10544-599
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100406
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, 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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