FDA APPLICATION 217844 | FDA Orange Book | Approved Drug Product List | PharmaCompass.com

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EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

PRESENTATION(s)

Product List 2024, Corporate Presentation, Manufacturing Sites and R&D Center, GMP Certificate 2021

Product List 2024
Corporate Presentation
Manufacturing Sites and R&D Center
GMP Certificate 2021

DIGITAL CONTENT

4 CORPORATE CONTENT #SupplierSpotlight, 245 NEWS #PharmaBuzz

4 CORPORATE CONTENT #SupplierSpotlight
245 NEWS #PharmaBuzz

DEVELOPMENTS

46 Drugs in Development

46 Drugs in Development

FINISHED DOSAGE FORMULATIONS

1168 FDF Dossiers, 509 FDA Orange Book, 2 Europe, 1 Canada, 77 Australia, 70 South Africa, 509 Listed Dossiers

1168 FDF Dossiers
509 FDA Orange Book
2 Europe
1 Canada
77 Australia
70 South Africa
509 Listed Dossiers

KEY PRODUCTS

Cyclosporine, Hydrocortisone, Hydrocortisone Acetate, Hydrocortisone Butyrate, Hydrocortisone Sodium Succinate, Hydrocortisone Valerate, Macrogol, Oseltamivir Phosphate, Vancomycin Hydrochloride

Cyclosporine
Hydrocortisone
Hydrocortisone Acetate
Hydrocortisone Butyrate
Hydrocortisone Sodium Succinate
Hydrocortisone Valerate
Macrogol
Oseltamivir Phosphate
Vancomycin Hydrochloride

INSPECTIONS & REGISTRATIONS

26 FDA, 12 EDQM, 2 WHO-GMP, 6 GDUFA

26 FDA
12 EDQM
2 WHO-GMP
6 GDUFA

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Brand Name : ICOSAPENT ETHYL

CPhI India 2024

Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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RLD : No

TE Code : AB

ICOSAPENT ETHYL

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Dosage Form : CAPSULE; ORAL

Proprietary Name : ICOSAPENT ETHYL

Dosage Strength : 500MG

Approval Date : 2023-09-22

Application Number : 217844

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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Brand Name : ICOSAPENT ETHYL

CPhI India 2024

Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Contact Supplier

Contact Supplier

Digital Content

RLD : No

TE Code : AB

ICOSAPENT ETHYL

Strides Pharma Science

Dosage Form : CAPSULE; ORAL

Proprietary Name : ICOSAPENT ETHYL

Dosage Strength : 1GM

Approval Date : 2023-09-22

Application Number : 217844

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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