Zambon Switzerland
FDA Approved Drugs

Zambon Switzerland

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 4
  • Latest Approval Date Dec 07, 2015
  • Data Source FDA
  • First Approval Date Dec 19, 1996
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Zambon Switzerland

Country

Switzerland

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Zambon Switzerland

Via Industria, 13 CH-6814 - Cadempino

Switzerland

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FDA Approved Drug Records ( 4 records )
2013
04 Dec
Discontinued Application: 91034

Drug Name

DORZOLAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE

Approval Date

2013-12-04

91034 / 1

Active Ingredient

DORZOLAMIDE HYDROCHLORIDE

Application Number

91034

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE

Approval Date

2013-12-04

Regulatory Status

Discontinued

2013
04 Dec
Discontinued Application: 91180

Drug Name

DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

2013-12-04

91180 / 1

Active Ingredient

DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

Application Number

91180

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

2013-12-04

Regulatory Status

Discontinued

1996
19 Dec
Discontinued Application: 50717

Drug Name

MONUROL

Product Number

1

Dosage Form

-

Strength

EQ 3GM BASE/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-12-19

50717 / 1

Active Ingredient

FOSFOMYCIN TROMETHAMINE

Application Number

50717

Product Number

1

Dosage Form

-

Strength

EQ 3GM BASE/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-12-19

Regulatory Status

Discontinued

2015
07 Dec
Discontinued Application: 204706

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2015-12-07

204706 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

204706

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

2015-12-07

Regulatory Status

Discontinued

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Drug Status Breakdown
4 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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Drug Name

DORZOLAMIDE HYDROCHLORIDE

Application Number

91034

Product Number

1

Active Ingredient

DORZOLAMIDE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 2% BASE

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