Bupropion Hydrochloride

Product NDC
71335-0612
11-digit product format
713350612
Labeler code
71335
Product ID
71335-0612_965030ad-13a2-4d23-9256-78bca2fea1a1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bupropion Hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075932
Marketing category
ANDA
Marketing start
2004-03-22
Marketing end
0000-00-00
Substance
BUPROPION HYDROCHLORIDE
Active strength
150 mg/1
Pharmacologic classes
Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
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
71335-0612-17133506120160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-1) 2010-07-120000-00-00NoNoCurrent
71335-0612-27133506120290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-2) 2010-07-120000-00-00NoNoCurrent
71335-0612-37133506120330 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-3) 2010-07-120000-00-00NoNoCurrent
71335-0612-471335061204120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-4) 2010-07-120000-00-00NoNoCurrent
71335-0612-57133506120545 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-5) 2010-07-120000-00-00NoNoCurrent
71335-0612-671335061206180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-6) 2010-07-120000-00-00NoNoCurrent
71335-0612-77133506120728 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-7) 2010-07-120000-00-00NoNoCurrent
71335-0612-87133506120856 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0612-8) 2010-07-120000-00-00NoNoCurrent