Glenwood
FDA Approved Drugs

Glenwood

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 6
  • Latest Approval Date Jan 01, 1982
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Glenwood

Country

Germany

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Glenwood

Arabellastraße, München, Bayern 81925

Germany

www.glenwood.de/ View on Map
FDA Approved Drug Records ( 6 records )
1982
01 Jan
Discontinued Application: 84188

Drug Name

MYOTONACHOL

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

84188 / 1

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84188

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84188

Drug Name

MYOTONACHOL

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84188 / 3

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84188

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84188

Drug Name

MYOTONACHOL

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84188 / 4

Active Ingredient

BETHANECHOL CHLORIDE

Application Number

84188

Product Number

4

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9395

Drug Name

PASKALIUM

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

1982-01-01

9395 / 3

Active Ingredient

POTASSIUM AMINOSALICYLATE

Application Number

9395

Product Number

3

Dosage Form

-

Strength

1GM

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 9395

Drug Name

PASKALIUM

Product Number

4

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

9395 / 4

Active Ingredient

POTASSIUM AMINOSALICYLATE

Application Number

9395

Product Number

4

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17569

Drug Name

RENOQUID

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

17569 / 1

Active Ingredient

SULFACYTINE

Application Number

17569

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
6 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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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

MYOTONACHOL

Application Number

84188

Product Number

1

Active Ingredient

BETHANECHOL CHLORIDE

Dosage Form

-

Strength

5MG

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