Roxybond

Product NDC
65597-502
11-digit product format
655970502
Labeler code
65597
Product ID
65597-502_eb44aa7a-4db6-42ab-9141-8dbf3742be60
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
oxycodone hydrochloride
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Daiichi Sankyo Inc.
Application
NDA209777
Marketing category
NDA
Marketing start
2017-04-20
Marketing end
0000-00-00
Substance
OXYCODONE HYDROCHLORIDE
Active strength
15 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65597-502-10EA - Each65597-5023e7ae1a5-92fd-4dca-bfd8-f424ede756a512018-07-03