Metaxalone

Product NDC
71335-1696
11-digit product format
713351696
Labeler code
71335
Product ID
71335-1696_fb5720e9-e309-43e5-b551-efc0fe933c85
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metaxalone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA204770
Marketing category
ANDA
Marketing start
2016-11-22
Marketing end
0000-00-00
Substance
METAXALONE
Active strength
800 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]
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 formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1696-071335169600100 TABLET in 1 BOTTLE (71335-1696-0) 100 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-17133516960130 TABLET in 1 BOTTLE (71335-1696-1) 30 tablet2020-09-030000-00-00NoNoCurrent
71335-1696-27133516960220 TABLET in 1 BOTTLE (71335-1696-2) 20 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-37133516960390 TABLET in 1 BOTTLE (71335-1696-3) 90 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-471335169604120 TABLET in 1 BOTTLE (71335-1696-4) 120 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-57133516960515 TABLET in 1 BOTTLE (71335-1696-5) 15 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-67133516960610 TABLET in 1 BOTTLE (71335-1696-6) 10 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-77133516960760 TABLET in 1 BOTTLE (71335-1696-7) 60 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-87133516960816 TABLET in 1 BOTTLE (71335-1696-8) 16 tablet2020-10-290000-00-00NoNoCurrent
71335-1696-97133516960984 TABLET in 1 BOTTLE (71335-1696-9) 84 tablet2020-10-290000-00-00NoNoCurrent