SB PHARMCO
FDA Approved Drugs

SB PHARMCO

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 30, 2007
  • Data Source FDA
  • First Approval Date Oct 10, 2002
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Company

SB PHARMCO

Country

U.S.A

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SB PHARMCO

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FDA Approved Drug Records ( 10 records )
2002
10 Oct
Discontinued Application: 21410

Drug Name

AVANDAMET

Product Number

1

Dosage Form

-

Strength

500MG;EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-10

21410 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

21410

Product Number

1

Dosage Form

-

Strength

500MG;EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-10

Regulatory Status

Discontinued

2002
10 Oct
Discontinued Application: 21410

Drug Name

AVANDAMET

Product Number

2

Dosage Form

-

Strength

500MG;EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-10

21410 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

21410

Product Number

2

Dosage Form

-

Strength

500MG;EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-10

Regulatory Status

Discontinued

2002
10 Oct
Discontinued Application: 21410

Drug Name

AVANDAMET

Product Number

3

Dosage Form

-

Strength

500MG;EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-10

21410 / 3

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

21410

Product Number

3

Dosage Form

-

Strength

500MG;EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-10-10

Regulatory Status

Discontinued

2003
25 Aug
Discontinued Application: 21410

Drug Name

AVANDAMET

Product Number

4

Dosage Form

-

Strength

1GM;EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-08-25

21410 / 4

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

21410

Product Number

4

Dosage Form

-

Strength

1GM;EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-08-25

Regulatory Status

Discontinued

2003
25 Aug
Discontinued Application: 21410

Drug Name

AVANDAMET

Product Number

5

Dosage Form

-

Strength

1GM;EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-08-25

21410 / 5

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Application Number

21410

Product Number

5

Dosage Form

-

Strength

1GM;EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-08-25

Regulatory Status

Discontinued

2005
23 Nov
Discontinued Application: 21700

Drug Name

AVANDARYL

Product Number

1

Dosage Form

-

Strength

1MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-11-23

21700 / 1

Active Ingredient

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Application Number

21700

Product Number

1

Dosage Form

-

Strength

1MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-11-23

Regulatory Status

Discontinued

2005
23 Nov
Discontinued Application: 21700

Drug Name

AVANDARYL

Product Number

2

Dosage Form

-

Strength

2MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-11-23

21700 / 2

Active Ingredient

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Application Number

21700

Product Number

2

Dosage Form

-

Strength

2MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-11-23

Regulatory Status

Discontinued

2005
23 Nov
Discontinued Application: 21700

Drug Name

AVANDARYL

Product Number

3

Dosage Form

-

Strength

4MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-11-23

21700 / 3

Active Ingredient

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Application Number

21700

Product Number

3

Dosage Form

-

Strength

4MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-11-23

Regulatory Status

Discontinued

2007
30 Mar
Discontinued Application: 21700

Drug Name

AVANDARYL

Product Number

4

Dosage Form

-

Strength

2MG;8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-03-30

21700 / 4

Active Ingredient

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Application Number

21700

Product Number

4

Dosage Form

-

Strength

2MG;8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-03-30

Regulatory Status

Discontinued

2007
30 Mar
Discontinued Application: 21700

Drug Name

AVANDARYL

Product Number

5

Dosage Form

-

Strength

4MG;8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-03-30

21700 / 5

Active Ingredient

GLIMEPIRIDE; ROSIGLITAZONE MALEATE

Application Number

21700

Product Number

5

Dosage Form

-

Strength

4MG;8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-03-30

Regulatory Status

Discontinued

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Drug Status Breakdown
10 total
  • Discontinued
Official Source

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FDA Approved Drug Record Details Preview

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

Drug Name

AVANDAMET

Application Number

21410

Product Number

1

Active Ingredient

METFORMIN HYDROCHLORIDE; ROSIGLITAZONE MALEATE

Dosage Form

-

Strength

500MG;EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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