OXECTA - 60793-526-01 - (OXYCODONE HYDROCHLORIDE)

Alphabetical Index


Drug Information of OXECTA

Product NDC: 60793-526
Proprietary Name: OXECTA
Non Proprietary Name: OXYCODONE HYDROCHLORIDE
Active Ingredient(s): 7.5    mg/1 & nbsp;   OXYCODONE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of OXECTA

Product NDC: 60793-526
Labeler Name: King Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202080
Marketing Category: NDA
Start Marketing Date: 20110617

Package Information of OXECTA

Package NDC: 60793-526-01
Package Description: 100 TABLET in 1 BOTTLE (60793-526-01)

NDC Information of OXECTA

NDC Code 60793-526-01
Proprietary Name OXECTA
Package Description 100 TABLET in 1 BOTTLE (60793-526-01)
Product NDC 60793-526
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYCODONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110617
Marketing Category Name NDA
Labeler Name King Pharmaceuticals, Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OXECTA


General Information