"0591-3739-10" National Drug Code (NDC)

Hydromorphone Hydrochloride 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3739-10)
(Actavis Pharma, Inc.)

NDC Code0591-3739-10
Package Description1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-3739-10)
Product NDC0591-3739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydromorphone Hydrochloride
Non-Proprietary NameHydromorphone Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140521
Marketing Category NameANDA
Application NumberANDA202144
ManufacturerActavis Pharma, Inc.
Substance NameHYDROMORPHONE HYDROCHLORIDE
Strength12
Strength Unitmg/1
Pharmacy ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0591-3739-10