RICONPHARMA LLC Discontinued
FDA Approved Drugs

RICONPHARMA LLC Discontinued

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 8
  • Latest Approval Date May 26, 2026
  • Data Source FDA
  • First Approval Date Apr 22, 2025
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Discontinued
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RX
9
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Company

RICONPHARMA LLC Discontinued

Country

U.S.A

Website

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RICONPHARMA LLC Discontinued

U.S.A

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FDA Approved Drug Records ( 8 records )
2025
22 Apr
Discontinued Application: 218444

Drug Name

SIPONIMOD

Product Number

1

Dosage Form

-

Strength

EQ 0.25MG BASE

Approval Date

2025-04-22

218444 / 1

Active Ingredient

SIPONIMOD

Application Number

218444

Product Number

1

Dosage Form

-

Strength

EQ 0.25MG BASE

Approval Date

2025-04-22

Regulatory Status

Discontinued

2025
22 Apr
Discontinued Application: 218444

Drug Name

SIPONIMOD

Product Number

2

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2025-04-22

218444 / 2

Active Ingredient

SIPONIMOD

Application Number

218444

Product Number

2

Dosage Form

-

Strength

EQ 1MG BASE

Approval Date

2025-04-22

Regulatory Status

Discontinued

2025
22 Apr
Discontinued Application: 218444

Drug Name

SIPONIMOD

Product Number

3

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2025-04-22

218444 / 3

Active Ingredient

SIPONIMOD

Application Number

218444

Product Number

3

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2025-04-22

Regulatory Status

Discontinued

2026
26 May
Discontinued Application: 220041

Drug Name

TOPIRAMATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2026-05-26

220041 / 1

Active Ingredient

TOPIRAMATE

Application Number

220041

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2026-05-26

Regulatory Status

Discontinued

2026
26 May
Discontinued Application: 220041

Drug Name

TOPIRAMATE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2026-05-26

220041 / 2

Active Ingredient

TOPIRAMATE

Application Number

220041

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2026-05-26

Regulatory Status

Discontinued

2026
26 May
Discontinued Application: 220041

Drug Name

TOPIRAMATE

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2026-05-26

220041 / 3

Active Ingredient

TOPIRAMATE

Application Number

220041

Product Number

3

Dosage Form

-

Strength

100MG

Approval Date

2026-05-26

Regulatory Status

Discontinued

2026
26 May
Discontinued Application: 220041

Drug Name

TOPIRAMATE

Product Number

4

Dosage Form

-

Strength

150MG

Approval Date

2026-05-26

220041 / 4

Active Ingredient

TOPIRAMATE

Application Number

220041

Product Number

4

Dosage Form

-

Strength

150MG

Approval Date

2026-05-26

Regulatory Status

Discontinued

2026
26 May
Discontinued Application: 220041

Drug Name

TOPIRAMATE

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

2026-05-26

220041 / 5

Active Ingredient

TOPIRAMATE

Application Number

220041

Product Number

5

Dosage Form

-

Strength

200MG

Approval Date

2026-05-26

Regulatory Status

Discontinued

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Drug Status Breakdown
8 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

SIPONIMOD

Application Number

218444

Product Number

1

Active Ingredient

SIPONIMOD

Dosage Form

-

Strength

EQ 0.25MG BASE

FDA Approved Drug Data

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Data maintained from official sources

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