ENDOCET - 60951-602-75 - (Oxycodone and Acetaminophen)

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Drug Information of ENDOCET

Product NDC: 60951-602
Proprietary Name: ENDOCET
Non Proprietary Name: Oxycodone and Acetaminophen
Active Ingredient(s): 325; 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 ENDOCET

Product NDC: 60951-602
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040330
Marketing Category: ANDA
Start Marketing Date: 20000526

Package Information of ENDOCET

Package NDC: 60951-602-75
Package Description: 5 BLISTER PACK in 1 BOX (60951-602-75) > 20 TABLET in 1 BLISTER PACK

NDC Information of ENDOCET

NDC Code 60951-602-75
Proprietary Name ENDOCET
Package Description 5 BLISTER PACK in 1 BOX (60951-602-75) > 20 TABLET in 1 BLISTER PACK
Product NDC 60951-602
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000526
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of ENDOCET


General Information