Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
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01 1Synnat Pharma
02 1LGM Pharma
03 1Aspen API
04 1Seqens
05 1Shanghai Minbiotech
06 2Farmhispania
07 1TAPI Technology & API Services
08 2Mankind Pharma
09 1Alkaloids Corporation
10 1Chengdu Xinhengchuang Pharmaceutical
11 1Curia
12 1Fuan Pharmaceutical
13 1GLAND CHEMICALS PRIVATE LIMITED
14 1GLAND PHARMA LIMITED
15 1Guangzhou Topwork Chemical
16 1Hameln rds
17 1Hanways Chempharm
18 1Harman Finochem
19 1Mac-Chem Products (India) Pvt.Ltd
20 1Mustafa Nevzat Ilac Sanayi A S
21 1Prajna Generics
22 1Reliance Life Sciences Private Limited
23 1Shenzhen Haorui
24 1Shenzhen HwaGen Pharmaceutical
25 1Shouyuan Chemical
26 1Sicor de Mexico
27 1Synbias Pharma
28 1Synthland
29 1Tecoland Corporation
30 1Teva Pharmaceutical Industries
31 1Viruj Pharmaceuticals Pvt Ltd
32 2Zhejiang Huahai Pharmaceutical
33 1Zhejiang Xianju Junye Pharmaceutical Co. LTD
34 1Zhejiang Xianju Pharmaceutical Co. Ltd
35 1Blank
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01 13China
02 1France
03 11India
04 2Israel
05 1Mexico
06 1Netherlands
07 1Slovakia
08 2Spain
09 1Switzerland
10 1Turkey
11 3U.S.A
12 1Blank
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01 12Active
02 1Inactive
03 25Blank
01 8Valid
02 1Withdrawn by Holder
03 29Blank
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01 1227MF10139
02 1227MF10199
03 1227MF10201
04 35Blank
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01 1WC-0353
02 1WC-0427A3-4
03 36Blank
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-30
Pay. Date : 2013-01-14
DMF Number : 9854
Submission : 1992-09-01
Status : Active
Type : II
Certificate Number : R1-CEP 2009-231 - Rev 02
Issue Date : 2022-11-25
Type : Chemical
Substance Number : 1764
Status : Valid
Registration Number : 227MF10199
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2015-08-06
Latest Date of Registration :
NDC Package Code : 60870-0450
Start Marketing Date : 1996-08-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF, CN |
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19572
Submission : 2006-06-29
Status : Active
Type : II
Available Reg Filing : EU DMF |
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-08-14
Pay. Date : 2018-07-27
DMF Number : 19819
Submission : 2006-09-15
Status : Active
Type : II
Certificate Number : R1-CEP 2006-176 - Rev 02
Issue Date : 2022-08-23
Type : Chemical
Substance Number : 1764
Status : Valid
Registration Number : 227MF10139
Registrant's Address : Balmes 85, Atico, 08008 (Barcelona), Spain
Initial Date of Registration : 2015-05-14
Latest Date of Registration :
NDC Package Code : 17404-1022
Start Marketing Date : 2008-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registrant Name : Pami Future Co., Ltd.
Registration Date : 2019-01-18
Registration Number : 20190118-210-J-304
Manufacturer Name : FARMHISPANIA, SA
Manufacturer Address : Passeig del Riu Besos, 9-10, 08160 MONTMELO (BARCELONA), SPAIN
Available Reg Filing : CN, RU |
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 : 2012-11-23
Pay. Date : 2012-11-13
DMF Number : 20068
Submission : 2006-12-20
Status : Active
Type : II
Available Reg Filing : BR, ASMF |
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 : 37698
Submission : 2023-01-05
Status : Active
Type : II
Certificate Number : CEP 2023-131 - Rev 02
Issue Date : 2025-01-21
Type : Chemical
Substance Number : 1764
Status : Valid
NDC Package Code : 17404-1022
Start Marketing Date : 2008-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registrant Name : Pami Future Co., Ltd.
Registration Date : 2019-01-18
Registration Number : 20190118-210-J-304
Manufacturer Name : FARMHISPANIA, SA
Manufacturer Address : Passeig del Riu Besos, 9-10, 08160 MONTMELO (BARCELONA), SPAIN
Available Reg Filing : CN, RU |
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-04-24
Pay. Date : 2024-04-08
DMF Number : 39437
Submission : 2024-03-28
Status : Active
Type : II
97
PharmaCompass offers a list of Rocuronium Bromide 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 Rocuronium Bromide manufacturer or Rocuronium Bromide supplier for your needs.
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A Rocuronium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rocuronium, including repackagers and relabelers. The FDA regulates Rocuronium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rocuronium 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 Rocuronium supplier is an individual or a company that provides Rocuronium active pharmaceutical ingredient (API) or Rocuronium finished formulations upon request. The Rocuronium suppliers may include Rocuronium API manufacturers, exporters, distributors and traders.
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We have 34 companies offering Rocuronium
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