EMD Serono Discontinued
FDA Approved Drugs

EMD Serono Discontinued

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.

Discontinued
  • Total Records 5
  • Latest Approval Date Dec 28, 1990
  • Data Source FDA
  • First Approval Date Mar 22, 1982
All
32
View
Unclassified
27
View
Discontinued
5
View
Company Overview

Company

EMD Serono Discontinued

Country

U.S.A

Website

Visit Website

Email

Social Profiles

LinkedIn X / Twitter
Company Snapshot

EMD Serono Discontinued

One Technology Place, Rockland, MA 02370

U.S.A

www.emdserono.com/us-en?global_redirect=1 View on Map
FDA Approved Drug Records ( 5 records )
1990
28 Dec
Discontinued Application: 19863

Drug Name

GEREF

Product Number

1

Dosage Form

-

Strength

EQ 0.05MG BASE/AMP **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1990-12-28

19863 / 1

Active Ingredient

SERMORELIN ACETATE

Application Number

19863

Product Number

1

Dosage Form

-

Strength

EQ 0.05MG BASE/AMP **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1990-12-28

Regulatory Status

Discontinued

1987
23 Dec
Discontinued Application: 19297

Drug Name

NOVANTRONE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/10ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-12-23

19297 / 1

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

19297

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/10ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-12-23

Regulatory Status

Discontinued

1987
23 Dec
Discontinued Application: 19297

Drug Name

NOVANTRONE

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE/12.5ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-12-23

19297 / 2

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

19297

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE/12.5ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-12-23

Regulatory Status

Discontinued

1987
23 Dec
Discontinued Application: 19297

Drug Name

NOVANTRONE

Product Number

3

Dosage Form

-

Strength

EQ 30MG BASE/15ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-12-23

19297 / 3

Active Ingredient

MITOXANTRONE HYDROCHLORIDE

Application Number

19297

Product Number

3

Dosage Form

-

Strength

EQ 30MG BASE/15ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-12-23

Regulatory Status

Discontinued

1982
22 Mar
Discontinued Application: 18361

Drug Name

SEROPHENE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-03-22

18361 / 1

Active Ingredient

CLOMIPHENE CITRATE

Application Number

18361

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-03-22

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    32 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
5 total
  • Discontinued
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

GEREF

Application Number

19863

Product Number

1

Active Ingredient

SERMORELIN ACETATE

Dosage Form

-

Strength

EQ 0.05MG BASE/AMP **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit