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"0781-5726-01" National Drug Code (NDC)
Oxycodone Hydrochloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5726-01)
(Sandoz Inc)
NDC Code
0781-5726-01
Package Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5726-01)
Product NDC
0781-5726
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Oxycodone Hydrochloride
Non-Proprietary Name
Oxycodone Hydrochloride
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20141008
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA022272
Manufacturer
Sandoz Inc
Substance Name
OXYCODONE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA Schedule
CII
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-5726-01