Sanofi
FDA Approved Drugs

Sanofi

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 RX
  • Total Records 11
  • Latest Approval Date Jul 16, 2021
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
11
View
Discontinued
10
View
RX
1
View
Company Overview

Company

Sanofi

Country

France

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Company Snapshot

Sanofi

54, rue La Boetie 75008 Paris

France

www.sanofi.com/en/your-health/specialty-care View on Map
FDA Approved Drug Records ( 11 records )
1982
01 Jan
Discontinued Application: 62278

Drug Name

CHLORAMPHENICOL SODIUM SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

62278 / 1

Active Ingredient

CHLORAMPHENICOL SODIUM SUCCINATE

Application Number

62278

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

2021
16 Jul
RX Application: 214429

Drug Name

FEXINIDAZOLE

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2021-07-16

214429 / 1

Active Ingredient

FEXINIDAZOLE

Application Number

214429

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

2021-07-16

Regulatory Status

RX

1997
15 Apr
Discontinued Application: 20579

Drug Name

FLOMAX

Product Number

1

Dosage Form

-

Strength

0.4MG

Approval Date

1997-04-15

20579 / 1

Active Ingredient

TAMSULOSIN HYDROCHLORIDE

Application Number

20579

Product Number

1

Dosage Form

-

Strength

0.4MG

Approval Date

1997-04-15

Regulatory Status

Discontinued

1999
09 Jun
Discontinued Application: 20862

Drug Name

HECTOROL

Product Number

1

Dosage Form

-

Strength

2.5MCG

Approval Date

1999-06-09

20862 / 1

Active Ingredient

DOXERCALCIFEROL

Application Number

20862

Product Number

1

Dosage Form

-

Strength

2.5MCG

Approval Date

1999-06-09

Regulatory Status

Discontinued

2004
23 Apr
Discontinued Application: 20862

Drug Name

HECTOROL

Product Number

2

Dosage Form

-

Strength

0.5MCG

Approval Date

2004-04-23

20862 / 2

Active Ingredient

DOXERCALCIFEROL

Application Number

20862

Product Number

2

Dosage Form

-

Strength

0.5MCG

Approval Date

2004-04-23

Regulatory Status

Discontinued

2009
13 Jul
Discontinued Application: 20862

Drug Name

HECTOROL

Product Number

3

Dosage Form

-

Strength

1MCG

Approval Date

2009-07-13

20862 / 3

Active Ingredient

DOXERCALCIFEROL

Application Number

20862

Product Number

3

Dosage Form

-

Strength

1MCG

Approval Date

2009-07-13

Regulatory Status

Discontinued

2000
06 Apr
Discontinued Application: 21027

Drug Name

HECTOROL

Product Number

1

Dosage Form

-

Strength

4MCG/2ML (2MCG/ML)

Approval Date

2000-04-06

21027 / 1

Active Ingredient

DOXERCALCIFEROL

Application Number

21027

Product Number

1

Dosage Form

-

Strength

4MCG/2ML (2MCG/ML)

Approval Date

2000-04-06

Regulatory Status

Discontinued

2000
06 Apr
Discontinued Application: 21027

Drug Name

HECTOROL

Product Number

2

Dosage Form

-

Strength

2MCG/ML (2MCG/ML)

Approval Date

2000-04-06

21027 / 2

Active Ingredient

DOXERCALCIFEROL

Application Number

21027

Product Number

2

Dosage Form

-

Strength

2MCG/ML (2MCG/ML)

Approval Date

2000-04-06

Regulatory Status

Discontinued

1984
31 Dec
Discontinued Application: 18719

Drug Name

MODRASTANE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1984-12-31

18719 / 1

Active Ingredient

TRILOSTANE

Application Number

18719

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

1984-12-31

Regulatory Status

Discontinued

1984
31 Dec
Discontinued Application: 18719

Drug Name

MODRASTANE

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

1984-12-31

18719 / 2

Active Ingredient

TRILOSTANE

Application Number

18719

Product Number

2

Dosage Form

-

Strength

30MG

Approval Date

1984-12-31

Regulatory Status

Discontinued

2007
19 Oct
Discontinued Application: 22127

Drug Name

RENVELA

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

2007-10-19

22127 / 1

Active Ingredient

SEVELAMER CARBONATE

Application Number

22127

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

2007-10-19

Regulatory Status

Discontinued

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Drug Status Breakdown
11 total
  • Discontinued
  • 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

CHLORAMPHENICOL SODIUM SUCCINATE

Application Number

62278

Product Number

1

Active Ingredient

CHLORAMPHENICOL SODIUM SUCCINATE

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

FDA Approved Drug Data

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