Pharmascience Inc. RX
FDA Approved Drugs

Pharmascience Inc. RX

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.

RX
  • Total Records 4
  • Latest Approval Date May 02, 2022
  • Data Source FDA
  • First Approval Date Mar 24, 2017
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RX
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Company Overview

Company

Pharmascience Inc. RX

Country

Canada

Social Profiles

Company Snapshot

Pharmascience Inc. RX

6111, Royalmount Avenue, Montreal, Quebec, H4P 2T4

Canada

www.pharmascience.com/ jcharland@pharmascience.com View on Map
FDA Approved Drug Records ( 4 records )
2022
02 May
RX Application: 208392

Drug Name

BORTEZOMIB

Product Number

1

Dosage Form

-

Strength

3.5MG/VIAL

Approval Date

2022-05-02

208392 / 1

Active Ingredient

BORTEZOMIB

Application Number

208392

Product Number

1

Dosage Form

-

Strength

3.5MG/VIAL

Approval Date

2022-05-02

Regulatory Status

RX

2017
24 Mar
RX Application: 207050

Drug Name

BUSULFAN

Product Number

1

Dosage Form

-

Strength

6MG/ML

Approval Date

2017-03-24

207050 / 1

Active Ingredient

BUSULFAN

Application Number

207050

Product Number

1

Dosage Form

-

Strength

6MG/ML

Approval Date

2017-03-24

Regulatory Status

RX

2017
31 May
RX Application: 204607

Drug Name

DECITABINE

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2017-05-31

204607 / 1

Active Ingredient

DECITABINE

Application Number

204607

Product Number

1

Dosage Form

-

Strength

50MG/VIAL

Approval Date

2017-05-31

Regulatory Status

RX

2017
08 Dec
RX Application: 207645

Drug Name

GANCICLOVIR SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2017-12-08

207645 / 1

Active Ingredient

GANCICLOVIR SODIUM

Application Number

207645

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2017-12-08

Regulatory Status

RX

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Drug Status Breakdown
4 total
  • RX
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Drug Name

BORTEZOMIB

Application Number

208392

Product Number

1

Active Ingredient

BORTEZOMIB

Dosage Form

-

Strength

3.5MG/VIAL

FDA Approved Drug Data

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