TRAMADOL HYDROCHLORIDE

Product NDC
10147-0902
11-digit product format
101470902
Labeler code
10147
Product ID
10147-0902_d2af68e8-c7e8-4adb-b1d9-6f25f32aba8a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
TRAMADOL HYDROCHLORIDE
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Patriot Pharmaceuticals, LLC
Application
NDA021692
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2006-01-16
Marketing end
0000-00-00
Substance
TRAMADOL HYDROCHLORIDE
Active strength
200 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CIV
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10147-0902-3EA - Each10147-090224396d38-6943-463d-a297-98afe782792212013-02-13