"0115-1234-03" National Drug Code (NDC)

Oxymorphone Hydrochloride 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-03)
(Amneal Pharmaceuticals of New York LLC)

NDC Code0115-1234-03
Package Description1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1234-03)
Product NDC0115-1234
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOxymorphone Hydrochloride
Non-Proprietary NameOxymorphone Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20130102
Marketing Category NameANDA
Application NumberANDA079087
ManufacturerAmneal Pharmaceuticals of New York LLC
Substance NameOXYMORPHONE HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCII

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