ENDOCET - 16590-925-83 - (OXYCODONE AND ACETAMINOPHEN)

Alphabetical Index


Drug Information of ENDOCET

Product NDC: 16590-925
Proprietary Name: ENDOCET
Non Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Active Ingredient(s): 325; 10    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: 16590-925
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040434
Marketing Category: ANDA
Start Marketing Date: 20030306

Package Information of ENDOCET

Package NDC: 16590-925-83
Package Description: 150 TABLET in 1 BOTTLE (16590-925-83)

NDC Information of ENDOCET

NDC Code 16590-925-83
Proprietary Name ENDOCET
Package Description 150 TABLET in 1 BOTTLE (16590-925-83)
Product NDC 16590-925
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYCODONE AND ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030306
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of ENDOCET


General Information