STERIMAX INC
FDA Approved Drugs

STERIMAX INC

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 9
  • Latest Approval Date Jun 09, 2020
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
9
View
Discontinued
8
View
RX
1
View
Company Overview

Company

STERIMAX INC

Country

Canada

Website

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Company Snapshot

STERIMAX INC

2770 PORTLAND DRIVE

Canada

sterimaxinc.com/ View on Map
FDA Approved Drug Records ( 9 records )
1982
01 Jan
Discontinued Application: 50547

Drug Name

CLAFORAN

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50547 / 1

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50547

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: 50547

Drug Name

CLAFORAN

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50547 / 2

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50547

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: 50547

Drug Name

CLAFORAN

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50547 / 3

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50547

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
29 Dec
Discontinued Application: 50547

Drug Name

CLAFORAN

Product Number

4

Dosage Form

-

Strength

EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-12-29

50547 / 4

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50547

Product Number

4

Dosage Form

-

Strength

EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-12-29

Regulatory Status

Discontinued

1985
20 May
Discontinued Application: 50596

Drug Name

CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

1985-05-20

50596 / 2

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50596

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

1985-05-20

Regulatory Status

Discontinued

1985
20 May
Discontinued Application: 50596

Drug Name

CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1985-05-20

50596 / 4

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50596

Product Number

4

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1985-05-20

Regulatory Status

Discontinued

1985
20 May
Discontinued Application: 50596

Drug Name

CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

1985-05-20

50596 / 1

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50596

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE/ML

Approval Date

1985-05-20

Regulatory Status

Discontinued

1985
20 May
Discontinued Application: 50596

Drug Name

CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1985-05-20

50596 / 3

Active Ingredient

CEFOTAXIME SODIUM

Application Number

50596

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1985-05-20

Regulatory Status

Discontinued

2020
09 Jun
RX Application: 208663

Drug Name

ETHACRYNATE SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

2020-06-09

208663 / 1

Active Ingredient

ETHACRYNATE SODIUM

Application Number

208663

Product Number

1

Dosage Form

-

Strength

EQ 50MG BASE/VIAL

Approval Date

2020-06-09

Regulatory Status

RX

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Drug Status Breakdown
9 total
  • Discontinued
  • 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

CLAFORAN

Application Number

50547

Product Number

1

Active Ingredient

CEFOTAXIME SODIUM

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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