Medicure
FDA Approved Drugs

Medicure

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 RX
  • Total Records 8
  • Latest Approval Date Jul 14, 2017
  • Data Source FDA
  • First Approval Date May 14, 1998
All
8
View
Discontinued
3
View
RX
5
View
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Medicure

Country

Canada

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Email

info@medicure.com

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Medicure

2-1250 Waverley Street Winnipeg, Manitoba R3T 6C6

Canada

www.medicure.com/ info@medicure.com View on Map
FDA Approved Drug Records ( 8 records )
1998
14 May
Discontinued Application: 20912

Drug Name

AGGRASTAT

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE/50ML (EQ 0.25MG BASE/ML)

Approval Date

1998-05-14

20912 / 1

Active Ingredient

TIROFIBAN HYDROCHLORIDE

Application Number

20912

Product Number

1

Dosage Form

-

Strength

EQ 12.5MG BASE/50ML (EQ 0.25MG BASE/ML)

Approval Date

1998-05-14

Regulatory Status

Discontinued

2016
31 Aug
RX Application: 20912

Drug Name

AGGRASTAT

Product Number

2

Dosage Form

-

Strength

EQ 3.75MG BASE/15ML (EQ 0.25MG BASE/ML)

Approval Date

2016-08-31

20912 / 2

Active Ingredient

TIROFIBAN HYDROCHLORIDE

Application Number

20912

Product Number

2

Dosage Form

-

Strength

EQ 3.75MG BASE/15ML (EQ 0.25MG BASE/ML)

Approval Date

2016-08-31

Regulatory Status

RX

1998
14 May
Discontinued Application: 20913

Drug Name

AGGRASTAT

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/500ML (EQ 0.05MG BASE/ML)

Approval Date

1998-05-14

20913 / 1

Active Ingredient

TIROFIBAN HYDROCHLORIDE

Application Number

20913

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE/500ML (EQ 0.05MG BASE/ML)

Approval Date

1998-05-14

Regulatory Status

Discontinued

2002
17 May
RX Application: 20913

Drug Name

AGGRASTAT

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/100ML (EQ 0.05MG BASE/ML)

Approval Date

2002-05-17

20913 / 2

Active Ingredient

TIROFIBAN HYDROCHLORIDE

Application Number

20913

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE/100ML (EQ 0.05MG BASE/ML)

Approval Date

2002-05-17

Regulatory Status

RX

2000
20 Apr
RX Application: 20913

Drug Name

AGGRASTAT

Product Number

3

Dosage Form

-

Strength

EQ 12.5MG BASE/250ML (EQ 0.05MG BASE/ML)

Approval Date

2000-04-20

20913 / 3

Active Ingredient

TIROFIBAN HYDROCHLORIDE

Application Number

20913

Product Number

3

Dosage Form

-

Strength

EQ 12.5MG BASE/250ML (EQ 0.05MG BASE/ML)

Approval Date

2000-04-20

Regulatory Status

RX

2017
14 Jul
Discontinued Application: 208379

Drug Name

ZYPITAMAG

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2017-07-14

208379 / 1

Active Ingredient

PITAVASTATIN MAGNESIUM

Application Number

208379

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2017-07-14

Regulatory Status

Discontinued

2017
14 Jul
RX Application: 208379

Drug Name

ZYPITAMAG

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2017-07-14

208379 / 2

Active Ingredient

PITAVASTATIN MAGNESIUM

Application Number

208379

Product Number

2

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2017-07-14

Regulatory Status

RX

2017
14 Jul
RX Application: 208379

Drug Name

ZYPITAMAG

Product Number

3

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2017-07-14

208379 / 3

Active Ingredient

PITAVASTATIN MAGNESIUM

Application Number

208379

Product Number

3

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2017-07-14

Regulatory Status

RX

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Drug Status Breakdown
8 total
  • Discontinued
  • RX
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

AGGRASTAT

Application Number

20912

Product Number

1

Active Ingredient

TIROFIBAN HYDROCHLORIDE

Dosage Form

-

Strength

EQ 12.5MG BASE/50ML (EQ 0.25MG BASE/ML)

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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