EMD Millipore Corporation RX
FDA Approved Drugs

EMD Millipore Corporation 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 3
  • Latest Approval Date Feb 03, 2021
  • Data Source FDA
  • First Approval Date Aug 11, 2000
All
27
View
Unclassified
2
View
Discontinued
22
View
RX
3
View
Company Overview

Company

EMD Millipore Corporation RX

Country

U.S.A

Email

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Company Snapshot

EMD Millipore Corporation RX

Burlington, Massachusetts 01803

U.S.A

www.emdmillipore.com/US/en View on Map
FDA Approved Drug Records ( 3 records )
2000
11 Aug
RX Application: 21197

Drug Name

CETROTIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.25MG BASE/VIAL

Approval Date

2000-08-11

21197 / 1

Active Ingredient

CETRORELIX ACETATE

Application Number

21197

Product Number

1

Dosage Form

-

Strength

EQ 0.25MG BASE/VIAL

Approval Date

2000-08-11

Regulatory Status

RX

2019
29 Mar
RX Application: 22561

Drug Name

MAVENCLAD

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2019-03-29

22561 / 1

Active Ingredient

CLADRIBINE

Application Number

22561

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2019-03-29

Regulatory Status

RX

2021
03 Feb
RX Application: 214096

Drug Name

TEPMETKO

Product Number

1

Dosage Form

-

Strength

EQ 225MG BASE

Approval Date

2021-02-03

214096 / 1

Active Ingredient

TEPOTINIB HYDROCHLORIDE

Application Number

214096

Product Number

1

Dosage Form

-

Strength

EQ 225MG BASE

Approval Date

2021-02-03

Regulatory Status

RX

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Drug Status Breakdown
3 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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FDA Approved Drug Record Details Preview

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

Drug Name

CETROTIDE

Application Number

21197

Product Number

1

Active Ingredient

CETRORELIX ACETATE

Dosage Form

-

Strength

EQ 0.25MG BASE/VIAL

FDA Approved Drug Data

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