Primlev - 24090-682-85 - (oxycodone and acetaminophen)

Alphabetical Index


Drug Information of Primlev

Product NDC: 24090-682
Proprietary Name: Primlev
Non Proprietary Name: oxycodone and acetaminophen
Active Ingredient(s): 300; 7.5    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 Primlev

Product NDC: 24090-682
Labeler Name: Akrimax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040608
Marketing Category: ANDA
Start Marketing Date: 20111201

Package Information of Primlev

Package NDC: 24090-682-85
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (24090-682-85)

NDC Information of Primlev

NDC Code 24090-682-85
Proprietary Name Primlev
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (24090-682-85)
Product NDC 24090-682
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111201
Marketing Category Name ANDA
Labeler Name Akrimax Pharmaceuticals, LLC
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 300; 7.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Primlev


General Information