FDA APPLICATION 210010 | 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, 253 NEWS #PharmaBuzz

4 CORPORATE CONTENT #SupplierSpotlight
253 NEWS #PharmaBuzz

DEVELOPMENTS

46 Drugs in Development

46 Drugs in Development

FINISHED DOSAGE FORMULATIONS

1082 FDF Dossiers, 462 FDA Orange Book, 2 Europe, 1 Canada, 83 Australia, 25 South Africa, 509 Listed Dossiers

1082 FDF Dossiers
462 FDA Orange Book
2 Europe
1 Canada
83 Australia
25 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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RANITIDINE HYDROCHLORIDE

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Dosage Form : TABLET; ORAL

Proprietary Name : RANITIDINE HYDROCHLORIDE

Dosage Strength : EQ 300MG BASE

Approval Date : 2018-08-01

Application Number : 210010

RX/OTC/DISCN : DISCN

RLD : No

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Brand Name : RANITIDINE HYDROCHLO...

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RLD : No

TE Code :

RANITIDINE HYDROCHLORIDE

Strides Pharma Science

Dosage Form : TABLET; ORAL

Proprietary Name : RANITIDINE HYDROCHLORIDE

Dosage Strength : EQ 150MG BASE

Approval Date : 2018-08-01

Application Number : 210010

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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