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OXYMORPHONE HYDROCHLORIDE - 0406-1009-01 - (Oxymorphone Hydrochloride)

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Drug Information of OXYMORPHONE HYDROCHLORIDE

Product NDC: 0406-1009
Proprietary Name: OXYMORPHONE HYDROCHLORIDE
Non Proprietary Name: Oxymorphone Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Oxymorphone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of OXYMORPHONE HYDROCHLORIDE

Product NDC: 0406-1009
Labeler Name: Mallinckrodt, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202321
Marketing Category: ANDA
Start Marketing Date: 20120412

Package Information of OXYMORPHONE HYDROCHLORIDE

Package NDC: 0406-1009-01
Package Description: 100 TABLET in 1 BOTTLE (0406-1009-01)

NDC Information of OXYMORPHONE HYDROCHLORIDE

NDC Code 0406-1009-01
Proprietary Name OXYMORPHONE HYDROCHLORIDE
Package Description 100 TABLET in 1 BOTTLE (0406-1009-01)
Product NDC 0406-1009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxymorphone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120412
Marketing Category Name ANDA
Labeler Name Mallinckrodt, Inc.
Substance Name OXYMORPHONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OXYMORPHONE HYDROCHLORIDE


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