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Oxycodone Hydchloride - 49999-899-00 - (Oxycodone Hydchloride)

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Drug Information of Oxycodone Hydchloride

Product NDC: 49999-899
Proprietary Name: Oxycodone Hydchloride
Non Proprietary Name: Oxycodone Hydchloride
Active Ingredient(s): 5    mg/1 & nbsp;   Oxycodone Hydchloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone Hydchloride

Product NDC: 49999-899
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091393
Marketing Category: ANDA
Start Marketing Date: 20111220

Package Information of Oxycodone Hydchloride

Package NDC: 49999-899-00
Package Description: 100 TABLET in 1 BOTTLE (49999-899-00)

NDC Information of Oxycodone Hydchloride

NDC Code 49999-899-00
Proprietary Name Oxycodone Hydchloride
Package Description 100 TABLET in 1 BOTTLE (49999-899-00)
Product NDC 49999-899
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydchloride
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 5
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydchloride


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