Extrovis AG RX
FDA Approved Drugs

Extrovis AG RX

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.

RX
  • Total Records 6
  • 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 RX

Country

Switzerland

Social Profiles

LinkedIn
Company Snapshot

Extrovis AG RX

Bahnhof-Park 4, Baar 6340

Switzerland

www.extrovis.com/ corporate@extrovis.com View on Map
FDA Approved Drug Records ( 6 records )
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

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
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

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

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Drug Status Breakdown
6 total
  • 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

CALCIUM CHLORIDE 10%

Application Number

219342

Product Number

1

Active Ingredient

CALCIUM CHLORIDE

Dosage Form

-

Strength

100MG/ML

FDA Approved Drug Data

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