NDC 54868-3671

NDC 54868-3671

NDC 54868-3671 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-3671
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-3671-2 [54868367102]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-12-17
Inactivation Date2019-09-24

NDC 54868-3671-0 [54868367100]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-12-17
Inactivation Date2019-09-24

NDC 54868-3671-3 [54868367103]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-12-17
Inactivation Date2019-09-24

NDC 54868-3671-1 [54868367101]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-12-17
Inactivation Date2019-09-24

NDC 54868-3671-5 [54868367105]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-04
Inactivation Date2019-09-24

NDC 54868-3671-7 [54868367107]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-05
Inactivation Date2019-09-24

NDC 54868-3671-6 [54868367106]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-04
Inactivation Date2019-09-24

NDC 54868-3671-4 [54868367104]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA075604
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-12-17
Inactivation Date2019-09-24

Drug Details

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