15 Jul 2024
// PRESS RELEASE
24 Jun 2024
// PRESS RELEASE
10 May 2024
// PRESS RELEASE
AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.
About
CPhI WW FrankfurtCPhI WW Frankfurt
Industry Trade Show
Booth #5.1C82
28-30 October, 2025
Industry Trade Show
Attending
03-06 November, 2025
Industry Trade Show
Attending
03-05 November, 2025
CONTACT DETAILS
Events
Webinars & Exhibitions
CPhI WW FrankfurtCPhI WW Frankfurt
Industry Trade Show
Booth #5.1C82
28-30 October, 2025
Industry Trade Show
Attending
03-06 November, 2025
Industry Trade Show
Attending
03-05 November, 2025
CORPORATE CONTENT #SupplierSpotlight
https://www.pharmacompass.com/radio-compass-blog/cdmo-activity-tracker-novo-s-parent-buys-catalent-for-us-16-5-bn-fujifilm-merck-kgaa-axplora-lonza-expand-capabilities
https://www.pharmacompass.com/radio-compass-blog/ophthalmic-dealmakers-novartis-abbvie-forge-deals-to-develop-ocular-gene-therapies
15 Jul 2024
// PRESS RELEASE
https://www.abbviecontractmfg.com/news-and-insights/success-factors-for-pre-filled-syringe-cmo-selection.html
24 Jun 2024
// PRESS RELEASE
https://www.abbviecontractmfg.com/news-and-insights/how-abbvie-operations-and-contract-manufacturing-has-prepared-global-parenteral-sites-for-the-annex-1-compliance-requirement.html
10 May 2024
// PRESS RELEASE
https://www.abbviecontractmfg.com/news-and-insights/translating-environmental-social-and-governance-esg-benefits-to-our-partners.html
20 Mar 2024
// PRESS RELEASE
https://www.abbviecontractmfg.com/news-and-insights/AbbVie-Contract-Manufacturing-12-Time-CMO-Leadership-Award-Winner.html#:~:text=AbbVie%20Contract%20Manufacturing%20%E2%80%93%2012%2DTime%20CMO%20Leadership%20Award%20Winner&text=AbbVie%20Contract%20Manufacturing%20has%20been,industry%20research%20and%20customer%20surveys.
11 Mar 2024
// PRESS RELEASE
https://www.abbviecontractmfg.com/news-and-insights/abbvie-contract-manufacturing-recognized-by-life-science-leader-for-the-11th-year.html
18 Jan 2024
// PRESS RELEASE
https://www.abbviecontractmfg.com/news-and-insights/Four-Myths-About-Embedded-CMOs-Busted.html
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13800
Submission : 1998-09-01
Status : Active
Type : II
Certificate Number : R1-CEP 1998-093 - Rev 07
Issue Date : 2020-10-09
Type : Chemical and TSE
Substance Number : 994
Status : Valid
NDC Package Code : 0074-5503
Start Marketing Date : 2010-05-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : AbbVie Korea Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-18-C-100-05
Manufacturer Name : AbbVie Inc.
Manufacturer Address : 1401 Sheridan Road, North Chicago, IL, 60064-4000, USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13197
Submission : 1998-04-30
Status : Active
Type : II
Certificate Number : R1-CEP 2016-267 - Rev 00
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 179
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-05-09
Pay. Date : 2013-09-25
DMF Number : 27155
Submission : 2015-11-10
Status : Active
Type : II
Certificate Number : R1-CEP 1997-001 - Rev 08
Issue Date : 2023-05-23
Type : Chemical
Substance Number : 179
Status : Valid
Certificate Number : R2-CEP 1995-038 - Rev 05
Issue Date : 2019-01-24
Type : Chemical
Substance Number : 1074
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8904
Submission : 1990-12-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13443
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13372
Submission : 1998-09-01
Status : Active
Type : II
Certificate Number : R1-CEP 2006-292 - Rev 00
Issue Date : 2012-09-24
Type : Chemical
Substance Number : 1673
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24315
Submission : 2010-11-30
Status : Active
Type : II
NDC Package Code : 68513-1054
Start Marketing Date : 2011-09-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2012-397 - Rev 00
Issue Date : 2019-09-19
Type : Chemical
Substance Number : 2136
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8904
Submission : 1990-12-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13800
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-05-09
Pay. Date : 2013-09-25
DMF Number : 27155
Submission : 2015-11-10
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13197
Submission : 1998-04-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13443
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13372
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24315
Submission : 2010-11-30
Status : Active
Type : II
Certificate Numbers : R2-CEP 1995-038 - Rev 05
Status : Valid
Issue Date : 2019-01-24
Type : Chemical
Substance Number : 1074
Certificate Numbers : R1-CEP 1998-093 - Rev 07
Status : Valid
Issue Date : 2020-10-09
Type : Chemical and TSE
Substance Number : 994
Certificate Numbers : R1-CEP 1997-001 - Rev 08
Status : Valid
Issue Date : 2023-05-23
Type : Chemical
Substance Number : 179
Certificate Numbers : R1-CEP 2016-267 - Rev 00
Status : Valid
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 179
Certificate Numbers : R1-CEP 2006-292 - Rev 00
Status : Valid
Issue Date : 2012-09-24
Type : Chemical
Substance Number : 1673
Certificate Numbers : R1-CEP 2012-397 - Rev 00
Status : Valid
Issue Date : 2019-09-19
Type : Chemical
Substance Number : 2136
Details:
Emraclidine is a Other Small Molecule drug candidate, which is currently being evaluated in Phase II clinical studies for the treatment of Schizophrenia.
Lead Product(s): Emraclidine,Inapplicable
Therapeutic Area: Psychiatry/Psychology Brand Name: Undisclosed
Study Phase: Phase IIProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 28, 2025
Lead Product(s) : Emraclidine,Inapplicable
Therapeutic Area : Psychiatry/Psychology
Highest Development Status : Phase II
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Emraclidine Safety, Disease Activity, PK In Adults with Schizophrenia
Details : Emraclidine is a Other Small Molecule drug candidate, which is currently being evaluated in Phase II clinical studies for the treatment of Schizophrenia.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
August 28, 2025
Details:
ABBV-8736 is a Antibody drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of unspecified medical condition.
Lead Product(s): ABBV-8736,Inapplicable
Therapeutic Area: Undisclosed Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Antibody, Unconjugated
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 26, 2025
Lead Product(s) : ABBV-8736,Inapplicable
Therapeutic Area : Undisclosed
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
ABBV-8736 IV Infusion Safety, Tolerability & PK In Healthy Adults
Details : ABBV-8736 is a Antibody drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of unspecified medical condition.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
August 26, 2025
Details:
AbbVie will GM-2505 (bretisilocin) acquire Gilgamesh's lead investigational candidate, currently in development for the treatment of patients with moderate-to-severe major depressive disorder.
Lead Product(s): Bretisilocin,Inapplicable
Therapeutic Area: Psychiatry/Psychology Brand Name: GM-2505
Study Phase: Phase IIProduct Type: Miscellaneous
Recipient: Gilgamesh Pharmaceuticals
Deal Size: $1,200.0 million Upfront Cash: Undisclosed
Deal Type: Acquisition August 25, 2025
Lead Product(s) : Bretisilocin,Inapplicable
Therapeutic Area : Psychiatry/Psychology
Highest Development Status : Phase II
Recipient : Gilgamesh Pharmaceuticals
Deal Size : $1,200.0 million
Deal Type : Acquisition
AbbVie to Acquire Gilgamesh Bretisilocin, a Novel, Investigational Therapy
Details : AbbVie will GM-2505 (bretisilocin) acquire Gilgamesh's lead investigational candidate, currently in development for the treatment of patients with moderate-to-severe major depressive disorder.
Product Name : GM-2505
Product Type : Miscellaneous
Upfront Cash : Undisclosed
August 25, 2025
Details:
ABBV-277 is a drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of unspecified medical condition.
Lead Product(s): ABBV-277,Inapplicable
Therapeutic Area: Undisclosed Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Undisclosed
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 22, 2025
Lead Product(s) : ABBV-277,Inapplicable
Therapeutic Area : Undisclosed
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Safety, PK, and Immunogenicity of ABBV-277 In Healthy Adults
Details : ABBV-277 is a drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of unspecified medical condition.
Product Name : Undisclosed
Product Type : Undisclosed
Upfront Cash : Inapplicable
August 22, 2025
Details:
Through the acqusition, Abbvie will leverage Capstan pipeline, including CPTX2309, anti-CD19 CAR-T therapy candidate, currently in Phase 1, in development for the treatment of autoimmune diseases.
Lead Product(s): CPTX2309,Inapplicable
Therapeutic Area: Immunology Brand Name: CPTX2309
Study Phase: Phase IProduct Type: Cell & Gene Therapy
Recipient: Capstan Therapeutics
Deal Size: $2,100.0 million Upfront Cash: $2,100.0 million
Deal Type: Acquisition August 19, 2025
Lead Product(s) : CPTX2309,Inapplicable
Therapeutic Area : Immunology
Highest Development Status : Phase I
Recipient : Capstan Therapeutics
Deal Size : $2,100.0 million
Deal Type : Acquisition
AbbVie Completes Acquisition of Capstan Therapeutics
Details : Through the acqusition, Abbvie will leverage Capstan pipeline, including CPTX2309, anti-CD19 CAR-T therapy candidate, currently in Phase 1, in development for the treatment of autoimmune diseases.
Product Name : CPTX2309
Product Type : Cell & Gene Therapy
Upfront Cash : $2,100.0 million
August 19, 2025
Details:
Etentamig is a Antibody drug candidate, which is currently being evaluated in Phase II/ Phase III clinical studies for the treatment of Multiple Myeloma.
Lead Product(s): Etentamig,Daratumumab,Lenalidomide,Dexamethasone
Therapeutic Area: Oncology Brand Name: Undisclosed
Study Phase: Phase II/ Phase IIIProduct Type: Antibody, Unconjugated
Sponsor: IFM (Intergroupe Français du Myélome) | PETHEMA (Program for the Study and Treatment of Haematological Malignances)
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 31, 2025
Lead Product(s) : Etentamig,Daratumumab,Lenalidomide,Dexamethasone
Therapeutic Area : Oncology
Highest Development Status : Phase II/ Phase III
Partner/Sponsor/Collaborator : IFM (Intergroupe Français du Myélome) | PETHEMA (Program for the Study and Treatment of Haematological Malignances)
Deal Size : Inapplicable
Deal Type : Inapplicable
Etentamig+Daratumumab vs DRd Safety & Disease Activity in NDMM Non-transplant Eligible
Details : Etentamig is a Antibody drug candidate, which is currently being evaluated in Phase II/ Phase III clinical studies for the treatment of Multiple Myeloma.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
July 31, 2025
Details:
Cyclophosphamide is a Cytotoxic Drug drug candidate, which is currently being evaluated in Phase II clinical studies for the treatment of Lymphoma, B-Cell.
Lead Product(s): Cyclophosphamide,Doxorubicin Hydrochloride,Epcoritamab,Etoposide,18-F Fludeoxyglucose,Prednisone,Rituximab
Therapeutic Area: Oncology Brand Name: Undisclosed
Study Phase: Phase IIProduct Type: Cytotoxic Drug
Recipient: University of Washington
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 31, 2025
Lead Product(s) : Cyclophosphamide,Doxorubicin Hydrochloride,Epcoritamab,Etoposide,18-F Fludeoxyglucose,Prednisone,Rituximab
Therapeutic Area : Oncology
Highest Development Status : Phase II
Recipient : University of Washington
Deal Size : Inapplicable
Deal Type : Inapplicable
Epcoritamab + Dose-Adjusted EPOCH-R Safety & Efficacy In Aggressive B-Cell NHL
Details : Cyclophosphamide is a Cytotoxic Drug drug candidate, which is currently being evaluated in Phase II clinical studies for the treatment of Lymphoma, B-Cell.
Product Name : Undisclosed
Product Type : Cytotoxic Drug
Upfront Cash : Inapplicable
July 31, 2025
Details:
Risankizumab is a Antibody drug candidate, which is currently being evaluated in Phase III clinical studies for the treatment of Colitis, Ulcerative.
Lead Product(s): Risankizumab,Inapplicable
Therapeutic Area: Immunology Brand Name: Undisclosed
Study Phase: Phase IIIProduct Type: Antibody, Unconjugated
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 17, 2025
Lead Product(s) : Risankizumab,Inapplicable
Therapeutic Area : Immunology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Risankizumab in Young Participants with Ulcerative Colitis
Details : Risankizumab is a Antibody drug candidate, which is currently being evaluated in Phase III clinical studies for the treatment of Colitis, Ulcerative.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
July 17, 2025
Details:
ABBV-932 is a drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of unspecified medical condition.
Lead Product(s): ABBV-932,Itraconazole
Therapeutic Area: Undisclosed Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Undisclosed
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 17, 2025
Lead Product(s) : ABBV-932,Itraconazole
Therapeutic Area : Undisclosed
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
ABBV-932 + Itraconazole Safety and PK In Healthy Adults
Details : ABBV-932 is a drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of unspecified medical condition.
Product Name : Undisclosed
Product Type : Undisclosed
Upfront Cash : Inapplicable
July 17, 2025
Details:
Mirvetuximab Soravtansine is a Antibody-drug Conjugate drug candidate, which is currently being evaluated in Phase II clinical studies for the treatment of Ovarian Neoplasms.
Lead Product(s): Mirvetuximab Soravtansine,Bevacizumab,Carboplatin
Therapeutic Area: Oncology Brand Name: Undisclosed
Study Phase: Phase IIProduct Type: Antibody-drug Conjugate
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 11, 2025
Lead Product(s) : Mirvetuximab Soravtansine,Bevacizumab,Carboplatin
Therapeutic Area : Oncology
Highest Development Status : Phase II
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
IV Mirvetuximab Soravtansine Safety & Disease Activity In Adult Ovarian Cancer Patients
Details : Mirvetuximab Soravtansine is a Antibody-drug Conjugate drug candidate, which is currently being evaluated in Phase II clinical studies for the treatment of Ovarian Neoplasms.
Product Name : Undisclosed
Product Type : Antibody-drug Conjugate
Upfront Cash : Inapplicable
July 11, 2025
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Powder For Solution For ...
Brand Name : Botox Allergan units
Dosage Strength :
Packaging :
Approval Date : 04/11/1994
Application Number : 52433
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Powder For Solution For ...
Brand Name : Botox Allergan units
Dosage Strength :
Packaging :
Approval Date : 04/11/1994
Application Number : 52433
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Powder For Solution For ...
Brand Name : Botox Allergan units
Dosage Strength :
Packaging :
Approval Date : 04/11/1994
Application Number : 52433
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Powder For Solution For ...
Brand Name : Vistabel
Dosage Strength :
Packaging :
Approval Date : 15/10/2002
Application Number : 55955
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Skyrizi
Dosage Strength : 150mg
Packaging :
Approval Date : 21/05/2021
Application Number : 20200728000052
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Skyrizi
Dosage Strength : 150mg
Packaging :
Approval Date : 21/05/2021
Application Number : 20200728000045
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Skyrizi
Dosage Strength : 180mg
Packaging :
Approval Date : 24/07/2024
Application Number : 20230828000034
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Skyrizi
Dosage Strength : 360mg
Packaging :
Approval Date : 21/11/2022
Application Number : 20211129000077
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Concentrate For Solution...
Brand Name : Skyrizi
Dosage Strength : 600mg
Packaging :
Approval Date : 21/11/2022
Application Number : 20211129000084
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Skyrizi
Dosage Strength : 75mg
Packaging :
Approval Date : 26/04/2019
Application Number : 20180430000079
Regulatory Info : Approved
Registration Country : Sweden
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : VICODIN HP
Dosage Strength : 660MG;10MG
Approval Date : 1996-09-23
Application Number : 40117
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : VICODIN
Dosage Strength : 500MG;5MG
Approval Date : 1983-01-07
Application Number : 88058
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : VICODIN ES
Dosage Strength : 750MG;7.5MG
Approval Date : 1988-12-09
Application Number : 89736
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : ACYCLOVIR
Dosage Strength : EQ 50MG BASE/ML
Approval Date : 1999-07-26
Application Number : 75114
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD :
TE Code :
Dosage Form : SYRINGE
Proprietary Name : HUMIRA
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 125057
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : VIAL
Proprietary Name : HUMIRA
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 125057
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : LASTACAFT
Dosage Strength : 0.25%
Approval Date : 2010-07-28
Application Number : 22134
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : SAPHRIS
Dosage Strength : EQ 5MG BASE
Approval Date : 2009-08-13
Application Number : 22117
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : SAPHRIS
Dosage Strength : EQ 10MG BASE
Approval Date : 2009-08-13
Application Number : 22117
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : SAPHRIS
Dosage Strength : EQ 2.5MG BASE
Approval Date : 2015-03-12
Application Number : 22117
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
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