TRAMADOL HYDROCHLORIDE

Product NDC
71335-1498
11-digit product format
713351498
Labeler code
71335
Product ID
71335-1498_f07c23d7-2797-4fac-b81b-ad0b9f878e41
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
TRAMADOL HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091498
Marketing category
ANDA
Marketing start
2015-05-22
Marketing end
0000-00-00
Substance
TRAMADOL HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1498-07133514980050 TABLET, FILM COATED in 1 BOTTLE (71335-1498-0) 2015-05-220000-00-00NoNoCurrent
71335-1498-17133514980130 TABLET, FILM COATED in 1 BOTTLE (71335-1498-1) 2015-05-220000-00-00NoNoCurrent
71335-1498-27133514980220 TABLET, FILM COATED in 1 BOTTLE (71335-1498-2) 2015-05-220000-00-00NoNoCurrent
71335-1498-37133514980390 TABLET, FILM COATED in 1 BOTTLE (71335-1498-3) 2015-05-220000-00-00NoNoCurrent
71335-1498-47133514980460 TABLET, FILM COATED in 1 BOTTLE (71335-1498-4) 2015-05-220000-00-00NoNoCurrent
71335-1498-571335149805120 TABLET, FILM COATED in 1 BOTTLE (71335-1498-5) 2015-05-220000-00-00NoNoCurrent
71335-1498-671335149806180 TABLET, FILM COATED in 1 BOTTLE (71335-1498-6) 2015-05-220000-00-00NoNoCurrent
71335-1498-77133514980740 TABLET, FILM COATED in 1 BOTTLE (71335-1498-7) 2015-05-220000-00-00NoNoCurrent
71335-1498-871335149808100 TABLET, FILM COATED in 1 BOTTLE (71335-1498-8) 2015-05-220000-00-00NoNoCurrent
71335-1498-97133514980915 TABLET, FILM COATED in 1 BOTTLE (71335-1498-9) 2015-05-220000-00-00NoNoCurrent