Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica
02 1Shandong Chenghui Shuangda Pharmaceutical
03 1Shandong Loncom Pharmaceutical
04 1Aesica Queenborough Limited
05 1Biotechnica DWC
06 1Cristalia Produtos Quimicos Farma. Ltda
07 1Dishman Carbogen Amcis
08 1Edmond Pharma
09 1Fresenius Kabi Oncology Limited
10 1Green Stone Swiss Co ., Ltd
11 2Pioneer Agro Extracts
12 1Remedy Labs
13 1Shiono Finesse
14 1Zhuhai Rundu Pharmaceutical
01 1Algeria
02 1Brazil
03 4China
04 6India
05 1Japan
06 1Spain
07 1United Kingdom
01 1Active
02 1Inactive
03 13Blank
01 15Blank
01 1218MF10003
02 1225MF10165
03 13Blank
01 1WC-0115
02 1WC-0174
03 1WC-0174A4
04 12Blank
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38858
Submission : 2023-09-26
Status : Active
Type : II
NDC Package Code : 66583-0815
Start Marketing Date : 2023-09-14
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 : 33982
Submission : 2019-08-20
Status : Inactive
Type : II
NDC Package Code : 61876-0728
Start Marketing Date : 2018-09-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Date of Issue : 2019-07-08
Valid Till : 2022-07-07
Written Confirmation Number : WC-0115
Address of the Firm :
Registration Number : 218MF10003
Registrant's Address : Queenborough, Kent ME11 5EL, United Kingdom
Initial Date of Registration : 2006-01-06
Latest Date of Registration :
Date of Issue : 2020-11-19
Valid Till : 2022-09-12
Written Confirmation Number : WC-0174A4
Address of the Firm :
Registration Number : 225MF10165
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 3-1-6
Initial Date of Registration : 2013-08-23
Latest Date of Registration :
Date of Issue : 2019-09-12
Valid Till : 2021-09-11
Written Confirmation Number : WC-0174
Address of the Firm :
A Levobupivacaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levobupivacaine Hydrochloride, including repackagers and relabelers. The FDA regulates Levobupivacaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levobupivacaine Hydrochloride 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 Levobupivacaine Hydrochloride supplier is an individual or a company that provides Levobupivacaine Hydrochloride active pharmaceutical ingredient (API) or Levobupivacaine Hydrochloride finished formulations upon request. The Levobupivacaine Hydrochloride suppliers may include Levobupivacaine Hydrochloride API manufacturers, exporters, distributors and traders.
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