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Oxycodone Hydrochloride - 0378-6113-01 - (Oxycodone Hydrochloride)

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Drug Information of Oxycodone Hydrochloride

Product NDC: 0378-6113
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 15    mg/1 & nbsp;   Oxycodone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone Hydrochloride

Product NDC: 0378-6113
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091313
Marketing Category: ANDA
Start Marketing Date: 20110228

Package Information of Oxycodone Hydrochloride

Package NDC: 0378-6113-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-6113-01)

NDC Information of Oxycodone Hydrochloride

NDC Code 0378-6113-01
Proprietary Name Oxycodone Hydrochloride
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-6113-01)
Product NDC 0378-6113
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110228
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


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