NDC 58118-1516

NDC 58118-1516

NDC 58118-1516 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-1516
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-1516-0 [58118151600]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1986-04-17
Marketing End Date2016-12-29

NDC 58118-1516-9 [58118151609]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1986-04-17
Marketing End Date2016-12-29

NDC 58118-1516-8 [58118151608]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1986-04-17
Marketing End Date2017-06-23

NDC 58118-1516-3 [58118151603]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1986-04-17
Marketing End Date2016-12-29

NDC 58118-1516-6 [58118151606]

Potassium Chloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1986-04-17
Marketing End Date2016-12-29

Drug Details

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