Future Pak LTD.
FDA Approved Drugs

Future Pak LTD.

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 2
  • Latest Approval Date Jan 25, 1993
  • Data Source FDA
  • First Approval Date Oct 22, 1987
Company Overview

Company

Future Pak LTD.

Country

U.S.A

Social Profiles

Company Snapshot

Future Pak LTD.

Future Pak 28115 Lakeview Drive Wixom, MI 48393, USA

U.S.A

www.futurepak.com/ sjmead@futurepak.com View on Map
FDA Approved Drug Records ( 2 records )
1987
22 Oct
Discontinued Application: 70999

Drug Name

K+10

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1987-10-22

70999 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

70999

Product Number

1

Dosage Form

-

Strength

10MEQ

Approval Date

1987-10-22

Regulatory Status

Discontinued

1993
25 Jan
Discontinued Application: 70998

Drug Name

K+8

Product Number

1

Dosage Form

-

Strength

8MEQ

Approval Date

1993-01-25

70998 / 1

Active Ingredient

POTASSIUM CHLORIDE

Application Number

70998

Product Number

1

Dosage Form

-

Strength

8MEQ

Approval Date

1993-01-25

Regulatory Status

Discontinued

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Drug Status Breakdown
2 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

K+10

Application Number

70999

Product Number

1

Active Ingredient

POTASSIUM CHLORIDE

Dosage Form

-

Strength

10MEQ

FDA Approved Drug Data

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