Bristol Myers Squibb Unclassified
FDA Approved Drugs

Bristol Myers Squibb Unclassified

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 12
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
217
View
Unclassified
12
View
Discontinued
182
View
RX
23
View
Company Overview

Company

Bristol Myers Squibb Unclassified

Country

U.S.A

Website

Visit Website

Email

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Bristol Myers Squibb Unclassified

430 E. 29th Street, 14th Floor, New York, NY 10016

U.S.A

www.bms.com/ View on Map
FDA Approved Drug Records ( 12 records )
-
Unclassified Application: 761035

Drug Name

EMPLICITI

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

761035 / 1

Active Ingredient

ELOTUZUMAB

Application Number

761035

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761035

Drug Name

EMPLICITI

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

-

761035 / 2

Active Ingredient

ELOTUZUMAB

Application Number

761035

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125288

Drug Name

NULOJIX

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

125288 / 1

Active Ingredient

BELATACEPT

Application Number

125288

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125527

Drug Name

OPDIVO

Product Number

1

Dosage Form

-

Strength

40MG/4ML

Approval Date

-

125527 / 1

Active Ingredient

NIVOLUMAB

Application Number

125527

Product Number

1

Dosage Form

-

Strength

40MG/4ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125527

Drug Name

OPDIVO

Product Number

2

Dosage Form

-

Strength

100MG/10ML

Approval Date

-

125527 / 2

Active Ingredient

NIVOLUMAB

Application Number

125527

Product Number

2

Dosage Form

-

Strength

100MG/10ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125554

Drug Name

OPDIVO

Product Number

1

Dosage Form

-

Strength

40MG/4ML

Approval Date

-

125554 / 1

Active Ingredient

NIVOLUMAB

Application Number

125554

Product Number

1

Dosage Form

-

Strength

40MG/4ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761234

Drug Name

OPDUALAG

Product Number

1

Dosage Form

-

Strength

240MG;80MG

Approval Date

-

761234 / 1

Active Ingredient

NIVOLUMAB;RELATLIMAB-RMBW

Application Number

761234

Product Number

1

Dosage Form

-

Strength

240MG;80MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125118

Drug Name

ORENCIA

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

125118 / 1

Active Ingredient

ABATACEPT

Application Number

125118

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 22072

Drug Name

SPRYCEL

Product Number

1

Dosage Form

-

Strength

70MG

Approval Date

-

22072 / 1

Active Ingredient

DASATINIB

Application Number

22072

Product Number

1

Dosage Form

-

Strength

70MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 125377

Drug Name

YERVOY

Product Number

1

Dosage Form

-

Strength

3MG

Approval Date

-

125377 / 1

Active Ingredient

IPILIMUMAB

Application Number

125377

Product Number

1

Dosage Form

-

Strength

3MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 221075

Drug Name

ZENBEXUS

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

-

221075 / 1

Active Ingredient

IBERDOMIDE

Application Number

221075

Product Number

1

Dosage Form

-

Strength

0.75MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 221075

Drug Name

ZENBEXUS

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

-

221075 / 2

Active Ingredient

IBERDOMIDE

Application Number

221075

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
12 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

EMPLICITI

Application Number

761035

Product Number

1

Active Ingredient

ELOTUZUMAB

Dosage Form

-

Strength

300MG

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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