Metaxalone

Product NDC
71335-0099
11-digit product format
713350099
Labeler code
71335
Product ID
71335-0099_3104ba9e-15ed-412f-9839-ecbcdf7bb282
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metaxalone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207466
Marketing category
ANDA
Marketing start
2017-08-31
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
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0099-071335009900100 TABLET in 1 BOTTLE (71335-0099-0) 100 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-17133500990130 TABLET in 1 BOTTLE (71335-0099-1) 30 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-27133500990220 TABLET in 1 BOTTLE (71335-0099-2) 20 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-37133500990390 TABLET in 1 BOTTLE (71335-0099-3) 90 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-471335009904120 TABLET in 1 BOTTLE (71335-0099-4) 120 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-57133500990515 TABLET in 1 BOTTLE (71335-0099-5) 15 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-67133500990610 TABLET in 1 BOTTLE (71335-0099-6) 10 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-77133500990760 TABLET in 1 BOTTLE (71335-0099-7) 60 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-87133500990816 TABLET in 1 BOTTLE (71335-0099-8) 16 tablet2017-09-260000-00-00NoNoCurrent
71335-0099-97133500990984 TABLET in 1 BOTTLE (71335-0099-9) 84 tablet2017-09-260000-00-00NoNoCurrent