Novo Nordisk
FDA Approved Drugs

Novo Nordisk

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 Discontinued
  • Total Records 4
  • Latest Approval Date Jun 22, 1998
  • Data Source FDA
  • First Approval Date Jun 22, 1998
All
4
View
Unclassified
2
View
Discontinued
2
View
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Company

Novo Nordisk

Country

Denmark

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Email

webmaster@novonordisk.com

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Novo Nordisk

Novo Allé, 2880 Bagsvaerd

Denmark

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FDA Approved Drug Records ( 4 records )
-
Unclassified Application: 21103

Drug Name

ACTIVELLA

Product Number

1

Dosage Form

-

Strength

1MG/0.5MG

Approval Date

-

21103 / 1

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Application Number

21103

Product Number

1

Dosage Form

-

Strength

1MG/0.5MG

Approval Date

-

Regulatory Status

Unclassified

1998
22 Jun
Discontinued Application: 20918

Drug Name

GLUCAGEN

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-06-22

20918 / 1

Active Ingredient

GLUCAGON HYDROCHLORIDE

Application Number

20918

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-06-22

Regulatory Status

Discontinued

1998
22 Jun
Discontinued Application: 20918

Drug Name

GLUCAGEN

Product Number

2

Dosage Form

-

Strength

EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-06-22

20918 / 2

Active Ingredient

GLUCAGON HYDROCHLORIDE

Application Number

20918

Product Number

2

Dosage Form

-

Strength

EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-06-22

Regulatory Status

Discontinued

-
Unclassified Application: 21878

Drug Name

LEVEMIR

Product Number

1

Dosage Form

-

Strength

100 UNITS/ML

Approval Date

-

21878 / 1

Active Ingredient

INSULIN DETEMIR

Application Number

21878

Product Number

1

Dosage Form

-

Strength

100 UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
4 total
  • Unclassified
  • 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

ACTIVELLA

Application Number

21103

Product Number

1

Active Ingredient

ESTRADIOL; NORETHINDRONE ACETATE

Dosage Form

-

Strength

1MG/0.5MG

FDA Approved Drug Data

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