LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 1Metrochem API Private Limited
03 4Dr. Reddy's Laboratories
04 1Gonane Pharma
05 1Jai Radhe Sales
06 1HRV Global Life Sciences
07 1Tenatra Chemie
08 1Anwita Drugs
09 2Aspire Lifesciences Pvt Ltd
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11 3Aurobindo Pharma Limited
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01 1173-26-ND
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-08-12
Pay. Date : 2012-11-30
DMF Number : 26475
Submission : 2012-10-03
Status : Active
Type : II
Date of Issue : 2022-06-15
Valid Till : 2025-06-16
Written Confirmation Number : WC-0034
Address of the Firm :
NDC Package Code : 55111-076
Start Marketing Date : 2012-08-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : EQ Bio Co., Ltd.
Registration Date : 2024-10-25
Registration Number : No. 4692-3-ND(3)
Manufacturer Name : Dr. Reddy's Laboratories Limited
Manufacturer Address : Chemical Technical Operations-Unit-II Plot No. 1, 75A, 75B, 105, 110, 111 & 112 Sri Venkateswara Co-operative Industrial Estate Bollaram, Jinnaram Mandal, Sangareddy District, Telangana, 502325 INDIA
Available Reg Filing : BR, ASMF, CA, RU |
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registrant Name : JDW Pharmaceutical Co., Ltd.
Registration Date : 2018-08-14
Registration Number : No. 4692-3-ND(2)
Manufacturer Name : Dr. Reddy\'s Laboratories Limited
Manufacturer Address : Chemical Technical Operations-Unit-II Plot No. 1, 75A, 75B, 105, 110, 111 & 112 Sri Venkateswara Co-operative Industrial Estate Bollaram, Jinnaram Mandal, Sangareddy District, Telangana, 502325 INDIA
Available Reg Filing : BR, ASMF, CA, RU |
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registrant Name : YuYu Pharmaceutical Co., Ltd.
Registration Date : 2011-09-02
Registration Number : No. 4692-3-ND(1)
Manufacturer Name : Dr. Reddy\'s Laboratories Limited
Manufacturer Address : Chemical Technical Operations-Unit-II Plot No. 1, 75A, 75B, 105, 110, 111 & 112 Sri Venkateswara Co-operative Industrial Estate Bollaram, Jinnaram Mandal, Sangareddy District, Telangana, 502325 INDIA
Available Reg Filing : BR, ASMF, CA, RU |
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registrant Name : Sangjin Corporation
Registration Date : 2010-12-30
Registration Number : No. 4692-3-ND
Manufacturer Name : Dr. Reddy\'s Laboratories Limited
Manufacturer Address : Chemical Technical Operations-Unit-II Plot No. 1, 75A, 75B, 105, 110, 111 & 112 Sri Venkateswara Co-operative Industrial Estate Bollaram, Jinnaram Mandal, Sangareddy District, Telangana, 502325 INDIA
Available Reg Filing : BR, ASMF, CA, RU |
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PharmaCompass offers a list of Dutasteride 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 Dutasteride manufacturer or Dutasteride supplier for your needs.
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A DUTASTERIDE [WHO-DD] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DUTASTERIDE [WHO-DD], including repackagers and relabelers. The FDA regulates DUTASTERIDE [WHO-DD] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DUTASTERIDE [WHO-DD] 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 DUTASTERIDE [WHO-DD] supplier is an individual or a company that provides DUTASTERIDE [WHO-DD] active pharmaceutical ingredient (API) or DUTASTERIDE [WHO-DD] finished formulations upon request. The DUTASTERIDE [WHO-DD] suppliers may include DUTASTERIDE [WHO-DD] API manufacturers, exporters, distributors and traders.
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