Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
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01 1Apex Healthcare Limited
02 1LGM Pharma
03 1Shandong Chenghui Shuangda Pharmaceutical
04 1Cambrex Corporation
05 1Dishman Carbogen Amcis
06 1Guangzhou Tosun Pharmaceutical
07 1Harman Finochem
08 1Ishita API
09 1Jiangsu Hengrui Medicine
10 1MSN Laboratories
11 1Nortec Quimica
12 1Parshwanath Life Sciences
13 1Siegfried AG
14 1Swati Spentose
15 1Themis Medicare
16 1Zhejiang Haichang Biomedical Technology
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01 1Brazil
02 4China
03 8India
04 1Switzerland
05 2U.S.A
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01 7Active
02 9Blank
01 1Valid
02 15Blank
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01 16Blank
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01 1WC-0457
02 15Blank
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01 120210113-210-J-819
02 15Blank
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01 112651-116
02 117381-024
03 157884-0038
04 159014-0053
05 161876-0727
06 172640-017
07 10Blank
01 16Blank
Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-08-06
Pay. Date : 2020-06-19
DMF Number : 34900
Submission : 2020-06-29
Status : Active
Type : II
NDC Package Code : 57884-0038
Start Marketing Date : 2020-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-10-05
Pay. Date : 2015-09-29
DMF Number : 19177
Submission : 2006-02-10
Status : Active
Type : II
Certificate Number : CEP 2025-114 - Rev 00
Issue Date : 2025-08-28
Type : Chemical
Substance Number : 2761
Status : Valid
NDC Package Code : 12651-116
Start Marketing Date : 2011-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-03-25
Pay. Date : 2018-11-13
DMF Number : 33285
Submission : 2018-11-21
Status : Active
Type : II
NDC Package Code : 59014-0053
Start Marketing Date : 2018-04-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-10-31
Pay. Date : 2014-10-23
DMF Number : 11938
Submission : 1996-04-18
Status : Active
Type : II
NDC Package Code : 17381-024
Start Marketing Date : 2010-04-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2025-03-07
Pay. Date : 2025-02-21
DMF Number : 41135
Submission : 2025-01-26
Status : Active
Type : II
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PharmaCompass offers a list of Bupivacaine 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 Bupivacaine manufacturer or Bupivacaine supplier for your needs.
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A DL-Bupivacaine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DL-Bupivacaine, including repackagers and relabelers. The FDA regulates DL-Bupivacaine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DL-Bupivacaine 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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We have 16 companies offering DL-Bupivacaine
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