NDC 16590-026

NDC 16590-026

NDC 16590-026 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 16590-026
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 16590-026-28 [16590002628]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-90 [16590002690]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-73 [16590002673]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-30 [16590002630]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-84 [16590002684]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-82 [16590002682]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-86 [16590002686]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-60 [16590002660]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-62 [16590002662]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

NDC 16590-026-72 [16590002672]

BACLOFEN TABLET
Marketing CategoryANDA
Application NumberANDA072824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-09-18
Inactivation Date2019-10-21

Drug Details

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