Apotex Fermentation Inc. Unclassified
FDA Approved Drugs

Apotex Fermentation Inc. Unclassified

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.

Unclassified
  • Total Records 9
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
558
View
Unclassified
9
View
Discontinued
263
View
OTC
8
View
RX
278
View
Company Overview

Company

Apotex Fermentation Inc. Unclassified

Country

Canada

Website

Visit Website

Email

services@apoferm.com

Social Profiles

Company Snapshot

Apotex Fermentation Inc. Unclassified

50 Scurfield BoulevardWinnipeg, ManitobaCanada R3Y 1G4

Canada

www.apoferm.com/ services@apoferm.com View on Map
FDA Approved Drug Records ( 9 records )
-
Unclassified Application: 78949

Drug Name

BUDESONIDE

Product Number

1

Dosage Form

-

Strength

0.032MG/INH

Approval Date

-

78949 / 1

Active Ingredient

BUDESONIDE

Application Number

78949

Product Number

1

Dosage Form

-

Strength

0.032MG/INH

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 209015

Drug Name

OLOPATADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.7% BASE

Approval Date

-

209015 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

209015

Product Number

1

Dosage Form

-

Strength

EQ 0.7% BASE

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 219399

Drug Name

RIMEGEPANT

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

-

219399 / 1

Active Ingredient

RIMEGEPANT

Application Number

219399

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 219660

Drug Name

Ruxolitinib

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

-

219660 / 2

Active Ingredient

Ruxolitinib

Application Number

219660

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 219660

Drug Name

Ruxolitinib

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

-

219660 / 3

Active Ingredient

Ruxolitinib

Application Number

219660

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 219660

Drug Name

Ruxolitinib

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

-

219660 / 4

Active Ingredient

Ruxolitinib

Application Number

219660

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 91378

Drug Name

SILDENAFIL CITRATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

-

91378 / 1

Active Ingredient

SILDENAFIL CITRATE

Application Number

91378

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 91378

Drug Name

SILDENAFIL CITRATE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

-

91378 / 2

Active Ingredient

SILDENAFIL CITRATE

Application Number

91378

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 91378

Drug Name

SILDENAFIL CITRATE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

-

91378 / 3

Active Ingredient

SILDENAFIL CITRATE

Application Number

91378

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
9 total
  • Unclassified
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

BUDESONIDE

Application Number

78949

Product Number

1

Active Ingredient

BUDESONIDE

Dosage Form

-

Strength

0.032MG/INH

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

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