RICONPHARMA LLC
FDA Approved Drugs
RICONPHARMA LLC
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.
- Total Records 17
- Latest Approval Date May 26, 2026
- Data Source FDA
- First Approval Date Nov 05, 2018
Company Snapshot
FDA Approved Drug Records ( 17 records )
Drug Name
COLESTIPOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
1GM
Approval Date
2024-12-03
Active Ingredient
COLESTIPOL HYDROCHLORIDE
Application Number
217462
Product Number
1
Dosage Form
-
Strength
1GM
Approval Date
2024-12-03
Regulatory Status
RX
Drug Name
FLUNISOLIDE
Product Number
1
Dosage Form
-
Strength
0.025MG/SPRAY
Approval Date
2022-06-16
Active Ingredient
FLUNISOLIDE
Application Number
207802
Product Number
1
Dosage Form
-
Strength
0.025MG/SPRAY
Approval Date
2022-06-16
Regulatory Status
RX
Drug Name
ISOSORBIDE MONONITRATE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2018-11-05
Active Ingredient
ISOSORBIDE MONONITRATE
Application Number
210918
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2018-11-05
Regulatory Status
RX
Drug Name
ISOSORBIDE MONONITRATE
Product Number
2
Dosage Form
-
Strength
60MG
Approval Date
2018-11-05
Active Ingredient
ISOSORBIDE MONONITRATE
Application Number
210918
Product Number
2
Dosage Form
-
Strength
60MG
Approval Date
2018-11-05
Regulatory Status
RX
Drug Name
ISOSORBIDE MONONITRATE
Product Number
3
Dosage Form
-
Strength
120MG
Approval Date
2018-11-05
Active Ingredient
ISOSORBIDE MONONITRATE
Application Number
210918
Product Number
3
Dosage Form
-
Strength
120MG
Approval Date
2018-11-05
Regulatory Status
RX
Drug Name
OXCARBAZEPINE
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2024-11-22
Active Ingredient
OXCARBAZEPINE
Application Number
215796
Product Number
1
Dosage Form
-
Strength
150MG
Approval Date
2024-11-22
Regulatory Status
RX
Drug Name
OXCARBAZEPINE
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2024-11-22
Active Ingredient
OXCARBAZEPINE
Application Number
215796
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
2024-11-22
Regulatory Status
RX
Drug Name
OXCARBAZEPINE
Product Number
3
Dosage Form
-
Strength
600MG
Approval Date
2024-11-22
Active Ingredient
OXCARBAZEPINE
Application Number
215796
Product Number
3
Dosage Form
-
Strength
600MG
Approval Date
2024-11-22
Regulatory Status
RX
Drug Name
SCOPOLAMINE
Product Number
1
Dosage Form
-
Strength
1MG/72HR
Approval Date
2020-11-24
Active Ingredient
SCOPOLAMINE
Application Number
212342
Product Number
1
Dosage Form
-
Strength
1MG/72HR
Approval Date
2020-11-24
Regulatory Status
RX
Drug Name
SIPONIMOD
Product Number
1
Dosage Form
-
Strength
EQ 0.25MG BASE
Approval Date
2025-04-22
Active Ingredient
SIPONIMOD
Application Number
218444
Product Number
1
Dosage Form
-
Strength
EQ 0.25MG BASE
Approval Date
2025-04-22
Regulatory Status
Discontinued
Drug Name
SIPONIMOD
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2025-04-22
Active Ingredient
SIPONIMOD
Application Number
218444
Product Number
2
Dosage Form
-
Strength
EQ 1MG BASE
Approval Date
2025-04-22
Regulatory Status
Discontinued
Drug Name
SIPONIMOD
Product Number
3
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2025-04-22
Active Ingredient
SIPONIMOD
Application Number
218444
Product Number
3
Dosage Form
-
Strength
EQ 2MG BASE
Approval Date
2025-04-22
Regulatory Status
Discontinued
Drug Name
TOPIRAMATE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2026-05-26
Active Ingredient
TOPIRAMATE
Application Number
220041
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2026-05-26
Regulatory Status
Discontinued
Drug Name
TOPIRAMATE
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2026-05-26
Active Ingredient
TOPIRAMATE
Application Number
220041
Product Number
2
Dosage Form
-
Strength
50MG
Approval Date
2026-05-26
Regulatory Status
Discontinued
Drug Name
TOPIRAMATE
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2026-05-26
Active Ingredient
TOPIRAMATE
Application Number
220041
Product Number
3
Dosage Form
-
Strength
100MG
Approval Date
2026-05-26
Regulatory Status
Discontinued
Drug Name
TOPIRAMATE
Product Number
4
Dosage Form
-
Strength
150MG
Approval Date
2026-05-26
Active Ingredient
TOPIRAMATE
Application Number
220041
Product Number
4
Dosage Form
-
Strength
150MG
Approval Date
2026-05-26
Regulatory Status
Discontinued
Drug Name
TOPIRAMATE
Product Number
5
Dosage Form
-
Strength
200MG
Approval Date
2026-05-26
Active Ingredient
TOPIRAMATE
Application Number
220041
Product Number
5
Dosage Form
-
Strength
200MG
Approval Date
2026-05-26
Regulatory Status
Discontinued
Drug Status Breakdown
17 total- RX
- 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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Explore important FDA approved drug information available in the records above.
Drug Name
COLESTIPOL HYDROCHLORIDE
Application Number
217462
Product Number
1
Active Ingredient
COLESTIPOL HYDROCHLORIDE
Dosage Form
-
Strength
1GM
FDA Approved Drug Data
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