Merck Serono
FDA Approved Drugs

Merck Serono

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.

Unclassified
  • Total Records 3
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
Company Overview

Company

Merck Serono

Country

Germany

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FDA Approved Drug Records ( 3 records )
-
Unclassified Application: 21120

Drug Name

NOVANTRONE

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

-

21120 / 1

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

21120

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103780

Drug Name

REBIF

Product Number

1

Dosage Form

-

Strength

22UG/0.5ML

Approval Date

-

103780 / 1

Active Ingredient

INTERFERON BETA-1A

Application Number

103780

Product Number

1

Dosage Form

-

Strength

22UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 103780

Drug Name

REBIF

Product Number

2

Dosage Form

-

Strength

44UG/0.5ML

Approval Date

-

103780 / 2

Active Ingredient

INTERFERON BETA-1A

Application Number

103780

Product Number

2

Dosage Form

-

Strength

44UG/0.5ML

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
3 total
  • Unclassified
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

NOVANTRONE

Application Number

21120

Product Number

1

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 2MG BASE/ML

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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