Key Therapeutics
FDA Approved Drugs

Key Therapeutics

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 4
  • Latest Approval Date Aug 04, 2017
  • Data Source FDA
  • First Approval Date Apr 28, 1983
Company Overview

Company

Key Therapeutics

Country

U.S.A

Website

Visit Website

Email

info@keytherapeutics.net

Social Profiles

Company Snapshot

Key Therapeutics

517 Liberty Rd suite d, Flowood, MS 39232

U.S.A

keytx.net/ info@keytherapeutics.net View on Map
FDA Approved Drug Records ( 4 records )
2017
04 Aug
Discontinued Application: 206615

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

300MG;50MG;40MG

Approval Date

2017-08-04

206615 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

206615

Product Number

1

Dosage Form

-

Strength

300MG;50MG;40MG

Approval Date

2017-08-04

Regulatory Status

Discontinued

1983
28 Apr
Discontinued Application: 88237

Drug Name

DEXAMETHASONE

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

1983-04-28

88237 / 1

Active Ingredient

DEXAMETHASONE

Application Number

88237

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

1983-04-28

Regulatory Status

Discontinued

2014
26 Nov
Discontinued Application: 204785

Drug Name

TREZIX

Product Number

1

Dosage Form

-

Strength

320.5MG;30MG;16MG

Approval Date

2014-11-26

204785 / 1

Active Ingredient

ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE

Application Number

204785

Product Number

1

Dosage Form

-

Strength

320.5MG;30MG;16MG

Approval Date

2014-11-26

Regulatory Status

Discontinued

2014
08 May
Discontinued Application: 204886

Drug Name

ZONTIVITY

Product Number

1

Dosage Form

-

Strength

EQ 2.08MG BASE

Approval Date

2014-05-08

204886 / 1

Active Ingredient

VORAPAXAR SULFATE

Application Number

204886

Product Number

1

Dosage Form

-

Strength

EQ 2.08MG BASE

Approval Date

2014-05-08

Regulatory Status

Discontinued

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Drug Status Breakdown
4 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

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Application Number

206615

Product Number

1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Dosage Form

-

Strength

300MG;50MG;40MG

FDA Approved Drug Data

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