Banner Pharmacaps Inc.
FDA Approved Drugs

Banner Pharmacaps 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
  • Total Records 10
  • Latest Approval Date Mar 20, 1992
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Banner Pharmacaps Inc.

Country

U.S.A

Website

Visit Website

Email

doingbusiness@patheon.com

Social Profiles

Company Snapshot

Banner Pharmacaps Inc.

4721 Emperor Blvd., Suite 200 Durham, NC 27703-8580

U.S.A

www.patheon.com/ doingbusiness@patheon.com View on Map
FDA Approved Drug Records ( 10 records )
1982
01 Jan
Discontinued Application: 84652

Drug Name

CHLOROTRIANISENE

Product Number

1

Dosage Form

-

Strength

12MG

Approval Date

1982-01-01

84652 / 1

Active Ingredient

CHLOROTRIANISENE

Application Number

84652

Product Number

1

Dosage Form

-

Strength

12MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1992
20 Mar
Discontinued Application: 73396

Drug Name

CLOFIBRATE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1992-03-20

73396 / 1

Active Ingredient

CLOFIBRATE

Application Number

73396

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1992-03-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84463

Drug Name

ETHCHLORVYNOL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84463 / 1

Active Ingredient

ETHCHLORVYNOL

Application Number

84463

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84463

Drug Name

ETHCHLORVYNOL

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84463 / 2

Active Ingredient

ETHCHLORVYNOL

Application Number

84463

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84463

Drug Name

ETHCHLORVYNOL

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

84463 / 3

Active Ingredient

ETHCHLORVYNOL

Application Number

84463

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84463

Drug Name

ETHCHLORVYNOL

Product Number

4

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

84463 / 4

Active Ingredient

ETHCHLORVYNOL

Application Number

84463

Product Number

4

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80702

Drug Name

VITAMIN A

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

80702 / 1

Active Ingredient

VITAMIN A PALMITATE

Application Number

80702

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83973

Drug Name

VITAMIN A

Product Number

1

Dosage Form

-

Strength

50,000USP UNITS

Approval Date

1982-01-01

83973 / 1

Active Ingredient

VITAMIN A

Application Number

83973

Product Number

1

Dosage Form

-

Strength

50,000USP UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83948

Drug Name

VITAMIN A PALMITATE

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

83948 / 1

Active Ingredient

VITAMIN A PALMITATE

Application Number

83948

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83981

Drug Name

VITAMIN A PALMITATE

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

83981 / 1

Active Ingredient

VITAMIN A PALMITATE

Application Number

83981

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
10 total
  • Discontinued
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

CHLOROTRIANISENE

Application Number

84652

Product Number

1

Active Ingredient

CHLOROTRIANISENE

Dosage Form

-

Strength

12MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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