NDC 54868-4617

NDC 54868-4617

NDC 54868-4617 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-4617
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-4617-4 [54868461704]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-04-19
Marketing End Date2012-09-05

NDC 54868-4617-1 [54868461701]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-04-19
Inactivation Date2019-09-24

NDC 54868-4617-5 [54868461705]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-04-19
Inactivation Date2019-09-24

NDC 54868-4617-3 [54868461703]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-04-19
Inactivation Date2019-09-24

NDC 54868-4617-0 [54868461700]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-04-19
Marketing End Date2012-05-04

NDC 54868-4617-2 [54868461702]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-04-19
Inactivation Date2019-09-24

Drug Details

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