Extrovis AG
FDA Approved Drugs

Extrovis AG

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 24
  • Latest Approval Date Apr 17, 2026
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
24
View
Discontinued
18
View
RX
6
View
Company Overview

Company

Extrovis AG

Country

Switzerland

Website

Visit Website

Email

corporate@extrovis.com

Social Profiles

LinkedIn
Company Snapshot

Extrovis AG

Bahnhof-Park 4, Baar 6340

Switzerland

www.extrovis.com/ corporate@extrovis.com View on Map
FDA Approved Drug Records ( 24 records )
2007
30 May
Discontinued Application: 65366

Drug Name

AZITHROMYCIN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2007-05-30

65366 / 1

Active Ingredient

AZITHROMYCIN

Application Number

65366

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2007-05-30

Regulatory Status

Discontinued

2024
27 Nov
RX Application: 219342

Drug Name

CALCIUM CHLORIDE 10%

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2024-11-27

219342 / 1

Active Ingredient

CALCIUM CHLORIDE

Application Number

219342

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2024-11-27

Regulatory Status

RX

2000
27 Oct
RX Application: 20985

Drug Name

CARAC

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2000-10-27

20985 / 1

Active Ingredient

FLUOROURACIL

Application Number

20985

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2000-10-27

Regulatory Status

RX

2016
25 May
Discontinued Application: 203063

Drug Name

CLINDAMYCIN PALMITATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/5ML

Approval Date

2016-05-25

203063 / 1

Active Ingredient

CLINDAMYCIN PALMITATE HYDROCHLORIDE

Application Number

203063

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/5ML

Approval Date

2016-05-25

Regulatory Status

Discontinued

1982
01 Jan
RX Application: 16831

Drug Name

EFUDEX

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

16831 / 1

Active Ingredient

FLUOROURACIL

Application Number

16831

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 16831

Drug Name

EFUDEX

Product Number

2

Dosage Form

-

Strength

5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16831 / 2

Active Ingredient

FLUOROURACIL

Application Number

16831

Product Number

2

Dosage Form

-

Strength

5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
RX Application: 16831

Drug Name

EFUDEX

Product Number

3

Dosage Form

-

Strength

5%

Approval Date

1982-01-01

16831 / 3

Active Ingredient

FLUOROURACIL

Application Number

16831

Product Number

3

Dosage Form

-

Strength

5%

Approval Date

1982-01-01

Regulatory Status

RX

2011
21 Dec
Discontinued Application: 200647

Drug Name

FLUDARABINE PHOSPHATE

Product Number

1

Dosage Form

-

Strength

50MG/2ML (25MG/ML)

Approval Date

2011-12-21

200647 / 1

Active Ingredient

FLUDARABINE PHOSPHATE

Application Number

200647

Product Number

1

Dosage Form

-

Strength

50MG/2ML (25MG/ML)

Approval Date

2011-12-21

Regulatory Status

Discontinued

2015
20 Apr
Discontinued Application: 203122

Drug Name

FLUOROURACIL

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2015-04-20

203122 / 1

Active Ingredient

FLUOROURACIL

Application Number

203122

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2015-04-20

Regulatory Status

Discontinued

2012
26 Nov
Discontinued Application: 201689

Drug Name

IFOSFAMIDE

Product Number

1

Dosage Form

-

Strength

1GM/20ML (50MG/ML)

Approval Date

2012-11-26

201689 / 1

Active Ingredient

IFOSFAMIDE

Application Number

201689

Product Number

1

Dosage Form

-

Strength

1GM/20ML (50MG/ML)

Approval Date

2012-11-26

Regulatory Status

Discontinued

2012
26 Nov
Discontinued Application: 201689

Drug Name

IFOSFAMIDE

Product Number

2

Dosage Form

-

Strength

3GM/60ML (50MG/ML)

Approval Date

2012-11-26

201689 / 2

Active Ingredient

IFOSFAMIDE

Application Number

201689

Product Number

2

Dosage Form

-

Strength

3GM/60ML (50MG/ML)

Approval Date

2012-11-26

Regulatory Status

Discontinued

2012
29 Mar
Discontinued Application: 201530

Drug Name

METHOTREXATE SODIUM PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/40ML (EQ 25MG BASE/ML)

Approval Date

2012-03-29

201530 / 1

Active Ingredient

METHOTREXATE SODIUM

Application Number

201530

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/40ML (EQ 25MG BASE/ML)

Approval Date

2012-03-29

Regulatory Status

Discontinued

2010
28 Jan
Discontinued Application: 90928

Drug Name

PEG 3350 AND ELECTROLYTES

Product Number

1

Dosage Form

-

Strength

236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

Approval Date

2010-01-28

90928 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

Application Number

90928

Product Number

1

Dosage Form

-

Strength

236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

Approval Date

2010-01-28

Regulatory Status

Discontinued

2010
02 Apr
Discontinued Application: 90409

Drug Name

PEG-3350, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CHLORIDE

Product Number

1

Dosage Form

-

Strength

420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

Approval Date

2010-04-02

90409 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

Application Number

90409

Product Number

1

Dosage Form

-

Strength

420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

Approval Date

2010-04-02

Regulatory Status

Discontinued

2026
17 Apr
RX Application: 220274

Drug Name

SODIUM ACETATE

Product Number

1

Dosage Form

-

Strength

100MEQ/50ML (2MEQ/ML)

Approval Date

2026-04-17

220274 / 1

Active Ingredient

SODIUM ACETATE

Application Number

220274

Product Number

1

Dosage Form

-

Strength

100MEQ/50ML (2MEQ/ML)

Approval Date

2026-04-17

Regulatory Status

RX

2026
17 Apr
RX Application: 220274

Drug Name

SODIUM ACETATE

Product Number

2

Dosage Form

-

Strength

200MEQ/100ML (2MEQ/ML)

Approval Date

2026-04-17

220274 / 2

Active Ingredient

SODIUM ACETATE

Application Number

220274

Product Number

2

Dosage Form

-

Strength

200MEQ/100ML (2MEQ/ML)

Approval Date

2026-04-17

Regulatory Status

RX

2016
29 Jun
Discontinued Application: 205227

Drug Name

TEMOZOLOMIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2016-06-29

205227 / 1

Active Ingredient

TEMOZOLOMIDE

Application Number

205227

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2016-06-29

Regulatory Status

Discontinued

2016
29 Jun
Discontinued Application: 205227

Drug Name

TEMOZOLOMIDE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2016-06-29

205227 / 2

Active Ingredient

TEMOZOLOMIDE

Application Number

205227

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2016-06-29

Regulatory Status

Discontinued

2016
29 Jun
Discontinued Application: 205227

Drug Name

TEMOZOLOMIDE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2016-06-29

205227 / 3

Active Ingredient

TEMOZOLOMIDE

Application Number

205227

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2016-06-29

Regulatory Status

Discontinued

2016
29 Jun
Discontinued Application: 205227

Drug Name

TEMOZOLOMIDE

Product Number

4

Dosage Form

-

Strength

140MG

Approval Date

2016-06-29

205227 / 4

Active Ingredient

TEMOZOLOMIDE

Application Number

205227

Product Number

4

Dosage Form

-

Strength

140MG

Approval Date

2016-06-29

Regulatory Status

Discontinued

2016
29 Jun
Discontinued Application: 205227

Drug Name

TEMOZOLOMIDE

Product Number

5

Dosage Form

-

Strength

180MG

Approval Date

2016-06-29

205227 / 5

Active Ingredient

TEMOZOLOMIDE

Application Number

205227

Product Number

5

Dosage Form

-

Strength

180MG

Approval Date

2016-06-29

Regulatory Status

Discontinued

2016
29 Jun
Discontinued Application: 205227

Drug Name

TEMOZOLOMIDE

Product Number

6

Dosage Form

-

Strength

250MG

Approval Date

2016-06-29

205227 / 6

Active Ingredient

TEMOZOLOMIDE

Application Number

205227

Product Number

6

Dosage Form

-

Strength

250MG

Approval Date

2016-06-29

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11600

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

11600 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

11600

Product Number

1

Dosage Form

-

Strength

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11600

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

3

Dosage Form

-

Strength

0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

11600 / 3

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

11600

Product Number

3

Dosage Form

-

Strength

0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

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
    24 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
24 total
  • Discontinued
  • RX
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

AZITHROMYCIN

Application Number

65366

Product Number

1

Active Ingredient

AZITHROMYCIN

Dosage Form

-

Strength

EQ 500MG BASE

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