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Last Updated: December 15, 2025

Details for New Drug Application (NDA): 070999

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NDA 070999 describes K+10, which is a drug marketed by Future Pak and is included in one NDA. Additional details are available on the K+10 profile page.

The generic ingredient in K+10 is potassium chloride. There are two hundred and forty drug master file entries for this compound. Eighty-five suppliers are listed for this compound. Additional details are available on the potassium chloride profile page.

Summary for 070999

Tradename:	K+10
Applicant:	Future Pak
Ingredient:	potassium chloride
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET, EXTENDED RELEASE;ORAL			Strength	10MEQ
Approval Date:	Oct 22, 1987	TE:		RLD:	No

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