04 Apr 2025
// PRESS RELEASE
03 Apr 2025
// PRESS RELEASE
29 Mar 2025
// PRESS RELEASE
Latest Content by PharmaCompass
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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09-11 April, 2025
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16-19 June, 2025
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CONTACT DETAILS
Events
Webinars & Exhibitions
Industry Trade Show
Not Confirmed
09-11 April, 2025
BIO International Conv...BIO International Convention
Industry Trade Show
Exhibiting
16-19 June, 2025
ChemOutsourcingChemOutsourcing
Industry Trade Show
Attending
08-10 September, 2025
CORPORATE CONTENT #SupplierSpotlight
https://www.pharmacompass.com/radio-compass-blog/top-first-in-class-drug-candidates-of-2025-ionis-donidalorsen-sanofi-s-fitusiran-cytokinetics-aficamten-await-fda-approval
https://www.pharmacompass.com/radio-compass-blog/fda-okays-50-new-drugs-in-2024-bms-cobenfy-lilly-s-kisunla-lead-pack-of-breakthrough-therapies
https://www.pharmacompass.com/radio-compass-blog/bms-j-j-bayer-lead-25-000-pharma-layoffs-in-2024-amylyx-fibrogen-kronos-bio-hit-by-trial-failures-cash-crunch
https://www.pharmacompass.com/radio-compass-blog/fda-s-landmark-approvals-of-bms-schizo-med-madrigal-s-mash-drug-us-16-5-bn-catalent-buyout-make-it-to-top-10-news-of-2024
https://www.pharmacompass.com/radio-compass-blog/chinese-fda-registered-generic-facilities-gain-steam-india-maintains-lead-with-396-facilities
https://www.pharmacompass.com/radio-compass-blog/medical-breakthroughs-in-2024-alzheimer-s-schizophrenia-copd-mash-see-pathbreaking-treatments
https://www.pharmacompass.com/radio-compass-blog/us-europe-turn-to-advanced-manufacturing-stockpiling-to-strengthen-drug-supply-chains
https://www.pharmacompass.com/radio-compass-blog/bms-bayer-takeda-pfizer-downsize-to-combat-cost-pressures-meet-restructuring-plans
https://www.pharmacompass.com/radio-compass-blog/novartis-gsk-sanofi-bms-shell-out-over-us-10-bn-in-dealmaking-as-mid-size-deals-take-centerstage-in-2024
https://www.pharmacompass.com/radio-compass-blog/fda-approvals-slump-19-in-h1-2024-nash-copd-pah-get-new-treatment-options
https://www.pharmacompass.com/radio-compass-blog/fda-s-june-2024-list-of-off-patent-off-exclusivity-drugs-sees-rise-in-cancer-hiv-treatments
04 Apr 2025
// PRESS RELEASE
https://www.sanofi.com/en/media-room/press-releases/2025/2025-04-03-05-00-00-3054815
03 Apr 2025
// PRESS RELEASE
https://ir.nurixtx.com/news-releases/news-release-details/nurix-licenses-drug-discovery-program-sanofi-targeting-novel
29 Mar 2025
// PRESS RELEASE
https://www.sanofi.com/en/media-room/press-releases/2025/2025-03-28-20-07-38-3051637
28 Mar 2025
// EXPRESSPHARMA
https://www.expresspharma.in/sanofis-mrna-vaccine-candidate-for-prevention-of-chlamydia-infection-gains-usfda-fast-track-designation/
28 Mar 2025
// GLOBENEWSWIRE
https://www.globenewswire.com/news-release/2025/03/28/3051139/0/en/Dupixent-dupilumab-Approved-as-the-First-ever-Biologic-Medicine-in-Japan-for-Patients-with-Chronic-Obstructive-Pulmonary-Disease-COPD.html
26 Mar 2025
// GLOBENEWSWIRE
https://www.globenewswire.com/news-release/2025/03/26/3049326/0/en/Press-Release-Chlamydia-vaccine-candidate-granted-fast-track-designation-by-the-US-FDA.html
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17115
Submission : 2004-01-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2399
Submission : 1975-02-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11994
Submission : 1996-06-04
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10996
Submission : 1994-07-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9957
Submission : 1992-11-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9382
Submission : 1991-10-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3593
Submission : 1979-06-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5148
Submission : 1983-11-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5048
Submission : 1983-07-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3142
Submission : 1978-02-01
Status : Inactive
Type : II
Registrant Name : Saehan Pharmaceutical Co., Ltd.
Registration Date : 2019-06-28
Registration Number : 20180516-7-K-33-01(1)
Manufacturer Name : Sanofi Winthrop Industrial@IND...
Manufacturer Address : Route d'Avignon 30390 ARAMON, France@38 Avenue Gustave Eiffel BP9528, TOURS, 37095
Registrant Name : Hanlim Pharmaceutical Co., Ltd.
Registration Date : 2018-05-16
Registration Number : 20180516-7-K-33-01
Manufacturer Name : Sanofi Winthrop Industrial@IND...
Manufacturer Address : Route d'Avignon 30390 ARAMON, France@38 avenue Gustave Eiffel BP9528, TOURS, 37095
Registrant Name : Korea Alcon Co., Ltd.
Registration Date : 2008-05-07
Registration Number : 20080507-96-E-55-14
Manufacturer Name : Genzyme Corporation
Manufacturer Address : 76 New York Avenue, Framingham, MA 01701-9322
Registrant Name : Sanofi-Aventis Korea Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-63-A-127-01
Manufacturer Name : EUROAPI ITALY SRL
Manufacturer Address : Via Angelo Titi 22/26 – 72100 Brindisi, Italy
NDC Package Code : 52465-105
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52465-104
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-6009
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-6007
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-7515
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-7800
Start Marketing Date : 2011-06-29
End Marketing Date : 2026-08-15
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-7004
Start Marketing Date : 2011-02-07
End Marketing Date : 2026-07-26
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-7902
Start Marketing Date : 2015-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-7900
Start Marketing Date : 2015-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50396-0201
Start Marketing Date : 2018-06-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Details:
Sanofi's chlamydia vaccine candidate is an mRNA-based prophylactic vaccine designed to prevent infections caused by the bacterium Chlamydia trachomatis.
Lead Product(s): Undisclosed
Therapeutic Area: Infections and Infectious Diseases Brand Name: Undisclosed
Study Phase: PreclinicalProduct Type: Vaccine
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable March 26, 2025
Lead Product(s) : Undisclosed
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Preclinical
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Chlamydia Vaccine Candidate Granted Fast Track Designation by the US FDA
Details : Sanofi's chlamydia vaccine candidate is an mRNA-based prophylactic vaccine designed to prevent infections caused by the bacterium Chlamydia trachomatis.
Product Name : Undisclosed
Product Type : Vaccine
Upfront Cash : Inapplicable
March 26, 2025
Details:
SAR442168 (tolebrutinib) is an investigational brain-penetrant and bioactive BTK inhibitor. Tolebrutinib is being evaluated for relapsing forms of MS, nrSPMS and PPMS.
Lead Product(s): Tolebrutinib
Therapeutic Area: Neurology Brand Name: SAR442168
Study Phase: Phase IIIProduct Type: Other Small Molecule
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable March 25, 2025
Lead Product(s) : Tolebrutinib
Therapeutic Area : Neurology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Tolebrutinib gets US Priority Review for Multiple Sclerosis
Details : SAR442168 (tolebrutinib) is an investigational brain-penetrant and bioactive BTK inhibitor. Tolebrutinib is being evaluated for relapsing forms of MS, nrSPMS and PPMS.
Product Name : SAR442168
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
March 25, 2025
Details:
Sarclisa (isatuximab) approved as a first anti-CD38 therapy in combination with Bortezomib and Dexamethasone soc treatment for patients with newly diagnosed transplant-ineligible multiple myeloma.
Lead Product(s): Isatuximab,Bortezomib
Therapeutic Area: Oncology Brand Name: Sarclisa
Study Phase: Approved FDFProduct Type: Antibody
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable February 25, 2025
Lead Product(s) : Isatuximab,Bortezomib
Therapeutic Area : Oncology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Sarclisa Approved in Japan for Patients with Newly Diagnosed Multiple Myeloma
Details : Sarclisa (isatuximab) approved as a first anti-CD38 therapy in combination with Bortezomib and Dexamethasone soc treatment for patients with newly diagnosed transplant-ineligible multiple myeloma.
Product Name : Sarclisa
Product Type : Antibody
Upfront Cash : Inapplicable
February 25, 2025
Details:
Dupixent (dupilumab) is a fully human monoclonal antibody that inhibits the signaling of the interleukin-4 (IL4) and interleukin-13 (IL13) pathways.
Lead Product(s): Dupilumab
Therapeutic Area: Immunology Brand Name: Dupixent
Study Phase: Phase II/ Phase IIIProduct Type: Antibody
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable February 18, 2025
Lead Product(s) : Dupilumab
Therapeutic Area : Immunology
Highest Development Status : Phase II/ Phase III
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Dupixent sBLA accepted for FDA priority review forbullous pemphigoid
Details : Dupixent (dupilumab) is a fully human monoclonal antibody that inhibits the signaling of the interleukin-4 (IL4) and interleukin-13 (IL13) pathways.
Product Name : Dupixent
Product Type : Antibody
Upfront Cash : Inapplicable
February 18, 2025
Details:
ExPEC9V (9-valent extraintestinal pathogenic escherichia coli vaccine) is being evaluated for invasive extraintestinal pathogenic escherichia coli disease in adults aged 60 years And older.
Lead Product(s): ExPEC9V
Therapeutic Area: Infections and Infectious Diseases Brand Name: VAC52416
Study Phase: Phase IIIProduct Type: Vaccine
Sponsor: Johnson & Johnson Innovative Medicine
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable February 17, 2025
Lead Product(s) : ExPEC9V
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Johnson & Johnson Innovative Medicine
Deal Size : Inapplicable
Deal Type : Inapplicable
Sanofi Updates on Extraintestinal Pathogenic E. Coli Vaccine Phase 3 Clinical Study
Details : ExPEC9V (9-valent extraintestinal pathogenic escherichia coli vaccine) is being evaluated for invasive extraintestinal pathogenic escherichia coli disease in adults aged 60 years And older.
Product Name : VAC52416
Product Type : Vaccine
Upfront Cash : Inapplicable
February 17, 2025
Details:
Merilog (insulin aspart) is rapid acting human insulin, which is indicated to improve glycemic control in adults and children with diabetes mellitus.
Lead Product(s): Insulin aspart
Therapeutic Area: Endocrinology Brand Name: Merilog
Study Phase: Approved FDFProduct Type: Hormone
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable February 14, 2025
Lead Product(s) : Insulin aspart
Therapeutic Area : Endocrinology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
FDA Approves First Rapid-Acting Insulin Biosimilar Product for Treatment of Diabetes
Details : Merilog (insulin aspart) is rapid acting human insulin, which is indicated to improve glycemic control in adults and children with diabetes mellitus.
Product Name : Merilog
Product Type : Hormone
Upfront Cash : Inapplicable
February 14, 2025
Details:
Rezurock (belumosudil mesylate), a prescription medicine used to treat adults and children 12 years of age and older with chronic graft-versus-host disease, is launched in India.
Lead Product(s): Belumosudil
Therapeutic Area: Immunology Brand Name: Rezurock
Study Phase: Approved FDFProduct Type: Other Small Molecule
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable February 10, 2025
Lead Product(s) : Belumosudil
Therapeutic Area : Immunology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Sanofi Launches Rezurock Against Chronic Graft-Versus-Host Disease in India
Details : Rezurock (belumosudil mesylate), a prescription medicine used to treat adults and children 12 years of age and older with chronic graft-versus-host disease, is launched in India.
Product Name : Rezurock
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
February 10, 2025
Details:
Sarclisa (isatuximab) approved as a first anti-CD38 therapy in combination with Bortezomib and Dexamethasone soc treatment for patients with newly diagnosed transplant-ineligible multiple myeloma.
Lead Product(s): Isatuximab,Bortezomib
Therapeutic Area: Oncology Brand Name: Sarclisa
Study Phase: Approved FDFProduct Type: Antibody
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable January 31, 2025
Lead Product(s) : Isatuximab,Bortezomib
Therapeutic Area : Oncology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Sarclisa Becomes First CD38 Therapy Approved in China for Myeloma
Details : Sarclisa (isatuximab) approved as a first anti-CD38 therapy in combination with Bortezomib and Dexamethasone soc treatment for patients with newly diagnosed transplant-ineligible multiple myeloma.
Product Name : Sarclisa
Product Type : Antibody
Upfront Cash : Inapplicable
January 31, 2025
Details:
Sarclisa (isatuximab) approved as a first anti-CD38 therapy in combination with Bortezomib and Dexamethasone soc treatment for patients with newly diagnosed transplant-ineligible multiple myeloma.
Lead Product(s): Isatuximab,Bortezomib
Therapeutic Area: Oncology Brand Name: Sarclisa
Study Phase: Approved FDFProduct Type: Antibody
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable January 22, 2025
Lead Product(s) : Isatuximab,Bortezomib
Therapeutic Area : Oncology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Sarclisa Approved in EU as First Anti-CD38 Therapy for Multiple Myeloma with VRd
Details : Sarclisa (isatuximab) approved as a first anti-CD38 therapy in combination with Bortezomib and Dexamethasone soc treatment for patients with newly diagnosed transplant-ineligible multiple myeloma.
Product Name : Sarclisa
Product Type : Antibody
Upfront Cash : Inapplicable
January 22, 2025
Details:
Sarclisa (isatuximab) is the first anti-CD38 therapy in combination with pomalidomide and Dexamethasone treatment for adult patients with multiple myeloma.
Lead Product(s): Isatuximab,Dexamethasone
Therapeutic Area: Oncology Brand Name: Sarclisa
Study Phase: Approved FDFProduct Type: Antibody
Sponsor: Inapplicable
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable January 13, 2025
Lead Product(s) : Isatuximab,Dexamethasone
Therapeutic Area : Oncology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Sarclisa Gets First Approval in China for Relapsed Multiple Myeloma
Details : Sarclisa (isatuximab) is the first anti-CD38 therapy in combination with pomalidomide and Dexamethasone treatment for adult patients with multiple myeloma.
Product Name : Sarclisa
Product Type : Antibody
Upfront Cash : Inapplicable
January 13, 2025
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Adult
Dosage Strength : 15mcg
Packaging : 0.5X1mcg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Adult
Dosage Strength : 15mcg
Packaging : 0.5X10mcg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Paed
Dosage Strength : 15mcg
Packaging : 0.5X1mcg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : PFS
Brand Name : Mutagrip
Dosage Strength : 15mcg
Packaging : 1X1mcg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Tetra
Dosage Strength : 15mcg
Packaging : 0.5X1mcg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Adult
Dosage Strength : 15mcg
Packaging : 0.5X1mcg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Adult
Dosage Strength : 15mcg
Packaging : 0.5X10mcg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Paed
Dosage Strength : 60mcg
Packaging : 0.5X1mcg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : INJ
Brand Name : Vaxigrip ® - Paed
Dosage Strength : 60mcg
Packaging : 0.5X1mcg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Dosage Form : PFS
Brand Name : Mutagrip
Dosage Strength : 15mcg
Packaging : 1X1mcg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
RLD : No
TE Code :
ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : TALACEN
Dosage Strength : 650MG;EQ 25MG BASE
Approval Date : 1982-09-23
Application Number : 18458
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD :
TE Code :
Dosage Form : VIAL; INTRAVENOUS
Proprietary Name : FABRAZYME
Dosage Strength : 5MG/VIAL
Approval Date :
Application Number : 103979
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : VIAL; INTRAVENOUS
Proprietary Name : FABRAZYME
Dosage Strength : 35MG/VIAL
Approval Date :
Application Number : 103979
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : VIAL; INTRAVENOUS
Proprietary Name : CAMPATH
Dosage Strength : 10MG/ML
Approval Date :
Application Number : 103948
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : VIAL; INTRAVENOUS
Proprietary Name : CAMPATH
Dosage Strength : 30MG/ML
Approval Date :
Application Number : 103948
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : LEMTRADA
Dosage Strength : 12MG/1.2ML (10MG/ML)
Approval Date :
Application Number : 103948
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : INJECTABLE; IV (INFUSION)
Proprietary Name : MYOZYME
Dosage Strength : 20MG/KG
Approval Date :
Application Number : 125141
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : POWDER; IV (INFUSION)
Proprietary Name : LUMIZYME
Dosage Strength : 5MG/ML
Approval Date :
Application Number : 125291
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : MYTELASE
Dosage Strength : 10MG
Approval Date : 1982-01-01
Application Number : 10155
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
ASPIRIN; PENTAZOCINE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : TALWIN COMPOUND
Dosage Strength : 325MG;EQ 12.5MG BASE **F...
Approval Date : 1982-01-01
Application Number : 16891
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Excipients
Inspections and registrations
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Sanofi-Aventis Deutschland GmbH is a supplier offers 202 products (APIs, Excipients or Intermediates).
Find a price of Irbesartan bulk with DMF, CEP, JDMF offered by Sanofi-Aventis Deutschland GmbH
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