VANSEN PHARMA
FDA Approved Drugs

VANSEN PHARMA

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 2
  • Latest Approval Date Jul 21, 2008
  • Data Source FDA
  • First Approval Date Aug 29, 2001
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VANSEN PHARMA

Country

Canada

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VANSEN PHARMA

Canada

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FDA Approved Drug Records ( 2 records )
2001
29 Aug
Discontinued Application: 21222

Drug Name

SPECTRACEF

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2001-08-29

21222 / 1

Active Ingredient

CEFDITOREN PIVOXIL

Application Number

21222

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2001-08-29

Regulatory Status

Discontinued

2008
21 Jul
Discontinued Application: 21222

Drug Name

SPECTRACEF

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2008-07-21

21222 / 2

Active Ingredient

CEFDITOREN PIVOXIL

Application Number

21222

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

2008-07-21

Regulatory Status

Discontinued

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Drug Status Breakdown
2 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

SPECTRACEF

Application Number

21222

Product Number

1

Active Ingredient

CEFDITOREN PIVOXIL

Dosage Form

-

Strength

200MG

FDA Approved Drug Data

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