Regeneron Pharmaceuticals
FDA Approved Drugs

Regeneron Pharmaceuticals

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 10
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
Company Overview

Company

Regeneron Pharmaceuticals

Country

U.S.A

Website

Visit Website

Email

Social Profiles

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Company Snapshot

Regeneron Pharmaceuticals

777 Old Saw Mill River Road Tarrytown, NY 10591

U.S.A

www.regeneron.com/ View on Map
FDA Approved Drug Records ( 10 records )
-
Unclassified Application: 761055

Drug Name

DUPIXENT

Product Number

1

Dosage Form

-

Strength

150MG/ML

Approval Date

-

761055 / 1

Active Ingredient

DUPILUMAB

Application Number

761055

Product Number

1

Dosage Form

-

Strength

150MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761181

Drug Name

EVKEEZA

Product Number

1

Dosage Form

-

Strength

345MG/2.3ML

Approval Date

-

761181 / 1

Active Ingredient

EVINACUMAB-DGNB

Application Number

761181

Product Number

1

Dosage Form

-

Strength

345MG/2.3ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761181

Drug Name

EVKEEZA

Product Number

2

Dosage Form

-

Strength

1200MG/8ML

Approval Date

-

761181 / 2

Active Ingredient

EVINACUMAB-DGNB

Application Number

761181

Product Number

2

Dosage Form

-

Strength

1200MG/8ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125387

Drug Name

EYLEA

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

-

125387 / 1

Active Ingredient

AFLIBERCEPT

Application Number

125387

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761355

Drug Name

EYLEA HD

Product Number

1

Dosage Form

-

Strength

8MG(0.07ML;114.3MG/ML)

Approval Date

-

761355 / 1

Active Ingredient

AFLIBERCEPT

Application Number

761355

Product Number

1

Dosage Form

-

Strength

8MG(0.07ML;114.3MG/ML)

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761169

Drug Name

INMAZEB

Product Number

1

Dosage Form

-

Strength

16.7MG/1ML

Approval Date

-

761169 / 1

Active Ingredient

ATOLTIVIMAB; ODESIVIMAB; MAFTIVIMAB

Application Number

761169

Product Number

1

Dosage Form

-

Strength

16.7MG/1ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761097

Drug Name

LIBTAYO

Product Number

1

Dosage Form

-

Strength

350MG

Approval Date

-

761097 / 1

Active Ingredient

CEMIPLIMAB-RWLC

Application Number

761097

Product Number

1

Dosage Form

-

Strength

350MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125559

Drug Name

PRALUENT

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

-

125559 / 1

Active Ingredient

ALIROCUMAB

Application Number

125559

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125559

Drug Name

PRALUENT

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

-

125559 / 2

Active Ingredient

ALIROCUMAB

Application Number

125559

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761339

Drug Name

VEOPOZ

Product Number

1

Dosage Form

-

Strength

400MG/2ML(200MG/ML)

Approval Date

-

761339 / 1

Active Ingredient

POZELIMAB-BBFG

Application Number

761339

Product Number

1

Dosage Form

-

Strength

400MG/2ML(200MG/ML)

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
10 total
  • Unclassified
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

DUPIXENT

Application Number

761055

Product Number

1

Active Ingredient

DUPILUMAB

Dosage Form

-

Strength

150MG/ML

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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