LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 1Jai Radhe Sales
03 1HRV Global Life Sciences
04 1Octavius Pharma Pvt. Ltd
05 1Tagoor Laboratories
06 1Tenatra Chemie
07 2TAPI Technology & API Services
08 1ACIC Europe API & Pharmaceuticals
09 2Dipharma
10 1F. Hoffmann-La Roche
11 2Industriale Chimica
12 1Mankind Pharma
13 1Nishchem International Pvt. Ltd
14 1Olon S.p.A
15 2R L Fine Chem
16 1Shouyuan Chemical
17 1Siegfried AG
18 1Sifavitor srl
19 1Sneha Medicare Pvt Ltd
20 1Sun Pharmaceutical Industries Limited
21 1Teva Pharmaceutical Industries
22 4Vasudha Pharma Chem
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01 1China
02 1Cyprus
03 15India
04 3Israel
05 6Italy
06 2Switzerland
07 1U.S.A
08 2Blank
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01 7Active
02 7Inactive
03 17Blank
01 1Expired
02 8Valid
03 22Blank
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01 1222MF10063
02 1302MF10137
03 29Blank
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01 1WC-0001
02 1WC-0001A4
03 3WC-0070
04 1WC-0139
05 1WC-0168
06 1WC-0445
07 1WC-287
08 22Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2001-432 - Rev 05
Issue Date : 2024-05-07
Type : Chemical
Substance Number : 464
Status : Valid
Registration Number : 302MF10137
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2020-11-26
Latest Date of Registration :
Date of Issue : 2022-06-22
Valid Till : 2025-05-20
Written Confirmation Number : WC-0001
Address of the Firm :
NDC Package Code : 15894-0033
Start Marketing Date : 2019-01-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Date of Issue : 2020-03-19
Valid Till : 2022-05-20
Written Confirmation Number : WC-0001A4
Address of the Firm :
NDC Package Code : 15894-0033
Start Marketing Date : 2019-01-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-09-16
Pay. Date : 2019-07-15
DMF Number : 33565
Submission : 2019-07-24
Status : Active
Type : II
Certificate Number : R0-CEP 2019-227 - Rev 00
Issue Date : 2021-07-16
Type : Chemical
Substance Number : 464
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-09-28
Pay. Date : 2015-09-21
DMF Number : 19635
Submission : 2006-07-28
Status : Active
Type : II
Certificate Number : R1-CEP 2013-323 - Rev 01
Issue Date : 2023-02-02
Type : Chemical
Substance Number : 464
Status : Valid
Date of Issue : 2022-06-14
Valid Till : 2025-07-04
Written Confirmation Number : WC-0070
Address of the Firm :
NDC Package Code : 66577-038
Start Marketing Date : 2018-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2019-08-06
Registration Number : 20130331-42-C-321-03(1)
Manufacturer Name : Vasudha Pharma Chem Limited
Manufacturer Address : Unit I, Plot No. 37/A, 38, 39A & B, Phase I IDA, Jeedimetla, Hyderabad-500 055, Telangana, India
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2598
Submission : 1976-01-28
Status : Active
Type : II
Registration Number : 222MF10063
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2010-02-22
Latest Date of Registration :
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-03-17
Pay. Date : 2017-03-02
DMF Number : 2719
Submission : 1976-08-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2908
Submission : 1977-03-18
Status : Active
Type : II
Certificate Number : R0-CEP 2019-193 - Rev 00
Issue Date : 2020-06-30
Type : Chemical
Substance Number : 464
Status : Valid
NDC Package Code : 46438-0038
Start Marketing Date : 1980-01-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-42-C-146-01
Manufacturer Name : Dipharma Francis Srl
Manufacturer Address : Via Bissone 5 20021 Baranzate Di Bollate(MI)_x000D_ _x000D_ _x000D_ 20021 Baranzate (MI), Italy
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-03-22
Pay. Date : 2016-09-26
DMF Number : 18111
Submission : 2005-02-10
Status : Active
Type : II
Certificate Number : CEP 2004-214 - Rev 05
Issue Date : 2024-04-03
Type : Chemical
Substance Number : 464
Status : Valid
Date of Issue : 2019-07-29
Valid Till : 2022-07-29
Written Confirmation Number : WC-0445
Address of the Firm :
NDC Package Code : 71554-001
Start Marketing Date : 2019-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19589
Submission : 2006-07-12
Status : Active
Type : II
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2413
Submission : 1975-03-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2535
Submission : 1975-10-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3449
Submission : 1979-02-26
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7802
Submission : 1988-11-28
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11027
Submission : 1994-07-21
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4311
Submission : 1981-10-19
Status : Inactive
Type : II
Date of Issue : 2019-07-22
Valid Till : 2022-07-22
Written Confirmation Number : WC-0139
Address of the Firm :
NDC Package Code : 71554-001
Start Marketing Date : 2019-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2004-263 - Rev 04
Issue Date : 2021-07-20
Type : Chemical
Substance Number : 464
Status : Valid
NDC Package Code : 17337-0501
Start Marketing Date : 2017-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2013-281 - Rev 00
Issue Date : 2021-03-23
Type : Chemical
Substance Number : 464
Status : Valid
NDC Package Code : 46438-0038
Start Marketing Date : 1980-01-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-42-C-146-01
Manufacturer Name : Dipharma Francis Srl
Manufacturer Address : Via Bissone 5 20021 Baranzate Di Bollate(MI)_x000D_ _x000D_ _x000D_ 20021 Baranzate (MI), Italy
Date of Issue : 2014-08-01
Valid Till : 2017-07-31
Written Confirmation Number : WC-287
Address of the Firm :
NDC Package Code : 66577-038
Start Marketing Date : 2018-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2019-08-06
Registration Number : 20130331-42-C-321-03(1)
Manufacturer Name : Vasudha Pharma Chem Limited
Manufacturer Address : Unit I, Plot No. 37/A, 38, 39A & B, Phase I IDA, Jeedimetla, Hyderabad-500 055, Telangana, India
Certificate Number : R0-CEP 2006-111 - Rev 00
Issue Date : 2008-05-30
Type : Chemical
Substance Number : 464
Status : Expired
Date of Issue : 2022-06-14
Valid Till : 2025-07-04
Written Confirmation Number : WC-0070
Address of the Firm :
NDC Package Code : 66577-038
Start Marketing Date : 2018-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2019-08-06
Registration Number : 20130331-42-C-321-03(1)
Manufacturer Name : Vasudha Pharma Chem Limited
Manufacturer Address : Unit I, Plot No. 37/A, 38, 39A & B, Phase I IDA, Jeedimetla, Hyderabad-500 055, Telangana, India
Date of Issue : 2022-06-14
Valid Till : 2025-07-04
Written Confirmation Number : WC-0070
Address of the Firm :
NDC Package Code : 66577-038
Start Marketing Date : 2018-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2019-08-06
Registration Number : 20130331-42-C-321-03(1)
Manufacturer Name : Vasudha Pharma Chem Limited
Manufacturer Address : Unit I, Plot No. 37/A, 38, 39A & B, Phase I IDA, Jeedimetla, Hyderabad-500 055, Telangana, India
64
PharmaCompass offers a list of Amitriptyline Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Amitriptyline Hydrochloride manufacturer or Amitriptyline Hydrochloride supplier for your needs.
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A Tryptizol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tryptizol, including repackagers and relabelers. The FDA regulates Tryptizol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tryptizol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tryptizol supplier is an individual or a company that provides Tryptizol active pharmaceutical ingredient (API) or Tryptizol finished formulations upon request. The Tryptizol suppliers may include Tryptizol API manufacturers, exporters, distributors and traders.
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We have 22 companies offering Tryptizol
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