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 1Ami Lifesciences Private Limited
04 1HRV Global Life Sciences
05 1Chunghwa Chemical Synthesis & Biotech
06 1Mankind Pharma
07 1Honour Lab
08 1Amara Labs
09 1Amino Chemicals
10 1Aurobindo Pharma Limited
11 1Aurore Life Sciences
12 1Bajaj Healthcare
13 1Biocon
14 1Bulat Pharmaceutical
15 2Changzhou Pharmaceutical Factory
16 1Chiral Quest
17 1DEAFARMA
18 2Harman Finochem
19 1Hetero Drugs
20 1Laurus Labs
21 1Lupin Ltd
22 2MSN Laboratories
23 1Prague Scientific
24 1Raks Pharma
25 1Unichem Laboratories Limited
26 2Viatris
27 1Viwit Pharmaceuticals Limited
28 1Zhejiang Jiuzhou Pharmaceutical
29 1Zhejiang Tianyu Pharmaceutical Co., Ltd
30 2Zhuhai Rundu Pharmaceutical
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01 8China
02 1Czech Republic
03 20India
04 1Italy
05 1Malta
06 1Taiwan
07 3U.S.A
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01 12Active
02 1Inactive
03 22Blank
01 35Blank
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01 35Blank
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01 1WC-0213
02 1WC-0362
03 2WC-0383
04 31Blank
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01 35Blank
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01 152076-6260
02 165727-079
03 169766-057
04 172023-0011
05 172023-0012
06 30Blank
01 35Blank
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.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38140
Submission : 2023-03-17
Status : Active
Type : II
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6260
Start Marketing Date : 2016-05-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36204
Submission : 2021-10-12
Status : Active
Type : II
Available Reg Filing : ASMF |
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
Date of Issue : 2023-11-28
Valid Till : 2025-05-05
Written Confirmation Number : WC-0362
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-06-04
Pay. Date : 2019-03-14
DMF Number : 33474
Submission : 2019-01-23
Status : Active
Type : II
NDC Package Code : 72023-0011
Start Marketing Date : 2024-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-05-28
Pay. Date : 2019-01-28
DMF Number : 33476
Submission : 2018-12-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41218
Submission : 2025-02-24
Status : Active
Type : II
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PharmaCompass offers a list of Sacubitril Sodium 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 Sacubitril Sodium manufacturer or Sacubitril Sodium supplier for your needs.
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A Sacubitril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sacubitril, including repackagers and relabelers. The FDA regulates Sacubitril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sacubitril 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 Sacubitril supplier is an individual or a company that provides Sacubitril active pharmaceutical ingredient (API) or Sacubitril finished formulations upon request. The Sacubitril suppliers may include Sacubitril API manufacturers, exporters, distributors and traders.
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We have 30 companies offering Sacubitril
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