Magnacet - 68453-992-10 - (oxycodone and acetaminophen)

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Drug Information of Magnacet

Product NDC: 68453-992
Proprietary Name: Magnacet
Non Proprietary Name: oxycodone and acetaminophen
Active Ingredient(s): 400; 5    mg/1; mg/1 & nbsp;   oxycodone and acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Magnacet

Product NDC: 68453-992
Labeler Name: Victory Pharma
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040687
Marketing Category: ANDA
Start Marketing Date: 20100330

Package Information of Magnacet

Package NDC: 68453-992-10
Package Description: 100 TABLET in 1 BOTTLE (68453-992-10)

NDC Information of Magnacet

NDC Code 68453-992-10
Proprietary Name Magnacet
Package Description 100 TABLET in 1 BOTTLE (68453-992-10)
Product NDC 68453-992
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100330
Marketing Category Name ANDA
Labeler Name Victory Pharma
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 400; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Magnacet


General Information