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Oxycodone Hydrochloride - 35356-212-90 - (Oxycodone Hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 35356-212
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 20    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: 35356-212
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077290
Marketing Category: ANDA
Start Marketing Date: 20111220

Package Information of Oxycodone Hydrochloride

Package NDC: 35356-212-90
Package Description: 90 TABLET in 1 BOTTLE (35356-212-90)

NDC Information of Oxycodone Hydrochloride

NDC Code 35356-212-90
Proprietary Name Oxycodone Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (35356-212-90)
Product NDC 35356-212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111220
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


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