Synthon Pharmaceuticals RX
FDA Approved Drugs

Synthon Pharmaceuticals 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 Sep 25, 2024
  • Data Source FDA
  • First Approval Date Apr 27, 2010
All
32
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Unclassified
2
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Discontinued
26
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RX
4
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Company Overview

Company

Synthon Pharmaceuticals RX

Country

Netherlands

Social Profiles

Company Snapshot

Synthon Pharmaceuticals RX

PO Box 70716503 GN NijmegenThe Netherlands

Netherlands

www.synthon.com/ communications@synthon.com View on Map
FDA Approved Drug Records ( 4 records )
2024
25 Sep
RX Application: 203857

Drug Name

GLATIRAMER ACETATE

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2024-09-25

203857 / 1

Active Ingredient

GLATIRAMER ACETATE

Application Number

203857

Product Number

1

Dosage Form

-

Strength

20MG/ML

Approval Date

2024-09-25

Regulatory Status

RX

2024
25 Sep
RX Application: 206873

Drug Name

GLATIRAMER ACETATE

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

2024-09-25

206873 / 1

Active Ingredient

GLATIRAMER ACETATE

Application Number

206873

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

2024-09-25

Regulatory Status

RX

2010
26 Nov
RX Application: 90229

Drug Name

LEVOCETIRIZINE DIHYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2010-11-26

90229 / 1

Active Ingredient

LEVOCETIRIZINE DIHYDROCHLORIDE

Application Number

90229

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2010-11-26

Regulatory Status

RX

2010
27 Apr
RX Application: 78801

Drug Name

TAMSULOSIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.4MG

Approval Date

2010-04-27

78801 / 1

Active Ingredient

TAMSULOSIN HYDROCHLORIDE

Application Number

78801

Product Number

1

Dosage Form

-

Strength

0.4MG

Approval Date

2010-04-27

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.

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

Drug Name

GLATIRAMER ACETATE

Application Number

203857

Product Number

1

Active Ingredient

GLATIRAMER ACETATE

Dosage Form

-

Strength

20MG/ML

FDA Approved Drug Data

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