NDC 0245-0180

NDC 0245-0180

NDC 0245-0180 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0245-0180
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0245-0180-11 [00245018011]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA078182
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-01-21
Marketing End Date2016-06-30

NDC 0245-0180-15 [00245018015]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA078182
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-01-21
Marketing End Date2016-06-30

NDC 0245-0180-89 [00245018089]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA078182
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-02-07
Marketing End Date2016-06-30

NDC 0245-0180-01 [00245018001]

Divalproex Sodium TABLET, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA078182
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-01-21
Marketing End Date2016-06-30

Drug Details

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.