LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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01 1LGM Pharma
02 2Cohance Lifesciences
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01 120181113-209-J-273
02 120181113-209-J-273(1)
03 120200707-209-J-548
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01 112666-0004
02 115308-1506
03 115308-2610
04 152286-0006
05 155111-098
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-11-03
Pay. Date : 2022-10-12
DMF Number : 34507
Submission : 2020-01-11
Status : Active
Type : II
Certificate Number : R1-CEP 2016-074 - Rev 01
Issue Date : 2022-12-16
Type : Chemical
Substance Number : 2119
Status : Valid
Date of Issue : 2025-07-24
Valid Till : 2028-07-21
Written Confirmation Number : WC-0150N
Address of the Firm :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-098
Start Marketing Date : 2005-05-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-04-10
Pay. Date : 2013-04-02
DMF Number : 17258
Submission : 2004-03-01
Status : Active
Type : II
NDC Package Code : 68069-0002
Start Marketing Date : 2009-10-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2021-04-16
Registration Number : 20210416-209-J-811
Manufacturer Name : Moehs Cantabra SL
Manufacturer Address : Poligono Industrial Requejada, Polanco 39313, Cantabria, Spain
| Available Reg Filing : ASMF |
Aarti Pharmalabs is a partner of choice for pharmaceutical companies for APIs & Intermediates. Largest Indian producer of Caffeine.
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-02-12
Pay. Date : 2016-01-28
DMF Number : 19879
Submission : 2006-10-11
Status : Active
Type : II
Certificate Number : R1-CEP 2009-082 - Rev 02
Issue Date : 2022-11-04
Type : Chemical
Substance Number : 2119
Status : Valid
Registration Number : 308MF10019
Registrant's Address : 204 Udyog Kshetra 2nd Floor Mulund-Goregaon Link Road, Mulund (W), Mumbai 400080, Maharashtra, INDIA
Initial Date of Registration : 2026-01-21
Latest Date of Registration :
Date of Issue : 2025-08-22
Valid Till : 2028-08-21
Written Confirmation Number : WC-0099
Address of the Firm :
NDC Package Code : 15308-1506
Start Marketing Date : 2012-12-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Myungin Pharmaceutical Co., Ltd.
Registration Date : 2019-01-07
Registration Number : 20181113-209-J-273(1)
Manufacturer Name : Aarti Pharmalabs limited Unit-IV
Manufacturer Address : Plot No. E-50, 50/1 & 59/1, MIDC, Tarapur, Taluka & District-Palghar 401506 Maharashtra State, India
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.
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-12-24
Pay. Date : 2012-11-13
DMF Number : 16281
Submission : 2002-12-02
Status : Active
Type : II
Certificate Number : CEP 2024-557 - Rev 00
Issue Date : 2025-03-24
Type : Chemical
Substance Number : 2119
Status : Valid
| Available Reg Filing : ASMF |
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PharmaCompass offers a list of Venlafaxine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Venlafaxine Hydrochloride manufacturer or Venlafaxine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Venlafaxine Hydrochloride manufacturer or Venlafaxine Hydrochloride supplier.
A Effexor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Effexor, including repackagers and relabelers. The FDA regulates Effexor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Effexor API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Effexor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Effexor supplier is an individual or a company that provides Effexor active pharmaceutical ingredient (API) or Effexor finished formulations upon request. The Effexor suppliers may include Effexor API manufacturers, exporters, distributors and traders.
click here to find a list of Effexor suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 71 companies offering Effexor
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