ALTANA
FDA Approved Drugs

ALTANA

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 12
  • Latest Approval Date Apr 01, 1998
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

ALTANA

Country

Denmark

Website

Visit Website

Email

Petra.Severit@altana.com

Social Profiles

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Company Snapshot

ALTANA

Abelstraße 43, Wesel, Nordrhein-Westfalen 46483, DE

Denmark

www.altana.com/ Petra.Severit@altana.com View on Map
FDA Approved Drug Records ( 12 records )
1982
01 Jan
Discontinued Application: 60731

Drug Name

BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE

Product Number

2

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1982-01-01

60731 / 2

Active Ingredient

BACITRACIN; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

60731

Product Number

2

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 60133

Drug Name

CHLORAMPHENICOL

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

60133 / 1

Active Ingredient

CHLORAMPHENICOL

Application Number

60133

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1998
01 Apr
Discontinued Application: 73440

Drug Name

DESOXIMETASONE

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1998-04-01

73440 / 1

Active Ingredient

DESOXIMETASONE

Application Number

73440

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1998-04-01

Regulatory Status

Discontinued

1991
23 Aug
Discontinued Application: 63107

Drug Name

EMGEL

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1991-08-23

63107 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

63107

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1991-08-23

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80489

Drug Name

HYDROCORTISONE

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

80489 / 2

Active Ingredient

HYDROCORTISONE

Application Number

80489

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80489

Drug Name

HYDROCORTISONE

Product Number

3

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

80489 / 3

Active Ingredient

HYDROCORTISONE

Application Number

80489

Product Number

3

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80848

Drug Name

HYDROCORTISONE

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

80848 / 2

Active Ingredient

HYDROCORTISONE

Application Number

80848

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80848

Drug Name

HYDROCORTISONE

Product Number

3

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

80848 / 3

Active Ingredient

HYDROCORTISONE

Application Number

80848

Product Number

3

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
20 Apr
Discontinued Application: 87273

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-04-20

87273 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

87273

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-04-20

Regulatory Status

Discontinued

1982
20 Apr
Discontinued Application: 87273

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-04-20

87273 / 2

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

87273

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-04-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83997

Drug Name

ZIPAN-25

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

83997 / 1

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

83997

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83997

Drug Name

ZIPAN-50

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

83997 / 2

Active Ingredient

PROMETHAZINE HYDROCHLORIDE

Application Number

83997

Product Number

2

Dosage Form

-

Strength

50MG/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
12 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

BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE

Application Number

60731

Product Number

2

Active Ingredient

BACITRACIN; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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