NDC 16590-220

NDC 16590-220

NDC 16590-220 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 16590-220
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 16590-220-30 [16590022030]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-56 [16590022056]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-90 [16590022090]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-60 [16590022060]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-62 [16590022062]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-84 [16590022084]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-28 [16590022028]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-20 [16590022020]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-75 [16590022075]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-86 [16590022086]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-72 [16590022072]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

NDC 16590-220-71 [16590022071]

TIZANIDINE TABLET
Marketing CategoryANDA
Application NumberANDA076286
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-07-03
Inactivation Date2019-11-13

Drug Details


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