LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 1Veranova
03 1HRV Global Life Sciences
04 1Shanghai Minbiotech
05 1TAPI Technology & API Services
06 1Andenex-Chemie Engelhard + Partner GmbH
07 1Aspen Bio
08 1Aspire Lifesciences Pvt Ltd
09 1Biotechnica DWC
10 1ChemGenix Laboratories Pvt Ltd
11 1Cipla
12 1Fresenius Kabi Oncology Limited
13 1Hanways Chempharm
14 1Heraeus Group
15 2Heraeus Holding
16 1Hetero Drugs
17 1Hospira, Inc.
18 1Hoventa Pharma
19 1IDT Australia Limited
20 1KUNMING GUIYAN PHARMACEUTICAL CO., LTD. CN 650 033 Kunming
21 1Laurus Labs
22 1Mac-Chem Products (India) Pvt.Ltd
23 1Nishchem International Pvt. Ltd
24 1Plantex Ltd.
25 1Qilu Pharmaceutical
26 1Sakar Healthcare
27 1Strem Chemicals
28 1Sun Pharmaceutical Industries Limited
29 1Surajlok Chemicals
30 1Tecoland Corporation
31 1Teva Pharmaceutical Industries
32 1Umicore
33 1Vinkem Labs Ltd
34 3Blank
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01 1Algeria
02 1Australia
03 4China
04 5Germany
05 15India
06 3Israel
07 5U.S.A
08 3Blank
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01 6Active
02 6Inactive
03 25Blank
01 1Expired
02 10Valid
03 2Withdrawn by Holder
04 24Blank
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01 1218MF10212
02 1222MF10106
03 35Blank
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01 1WC-0041
02 1WC-0159nA2
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01 120190410-210-J-334
02 120190410-210-J-334(1)
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01 149812-0009
02 154875-0001
03 167184-0010
04 168554-0077
05 172659-864
06 32Blank
01 37Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9601
Submission : 1992-03-26
Status : Active
Type : II
Certificate Number : CEP 2005-253 - Rev 02
Issue Date : 2025-01-22
Type : Chemical
Substance Number : 599
Status : Valid
Registration Number : 222MF10106
Registrant's Address : 435 Devon Park Drive, Suite 400, Wayne, Pennsylvania 19087 USA
Initial Date of Registration : 2010-03-19
Latest Date of Registration :
NDC Package Code : 49812-0009
Start Marketing Date : 1985-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
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 : 2014-10-21
Pay. Date : 2014-03-10
DMF Number : 28046
Submission : 2014-03-09
Status : Active
Type : II
Certificate Number : R1-CEP 2012-012 - Rev 00
Issue Date : 2018-06-01
Type : Chemical
Substance Number : 599
Status : Valid
NDC Package Code : 72659-864
Start Marketing Date : 2017-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7017
Submission : 1987-06-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4098
Submission : 1981-03-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4824
Submission : 1983-03-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23985
Submission : 2010-05-22
Status : Inactive
Type : II
Certificate Number : R1-CEP 2010-122 - Rev 02
Issue Date : 2021-09-16
Type : Chemical
Substance Number : 599
Status : Valid
NDC Package Code : 67184-0010
Start Marketing Date : 2023-11-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Cisplatin 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 Cisplatin manufacturer or Cisplatin supplier for your needs.
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A Cisplatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cisplatin, including repackagers and relabelers. The FDA regulates Cisplatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cisplatin 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 Cisplatin supplier is an individual or a company that provides Cisplatin active pharmaceutical ingredient (API) or Cisplatin finished formulations upon request. The Cisplatin suppliers may include Cisplatin API manufacturers, exporters, distributors and traders.
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We have 33 companies offering Cisplatin
Get in contact with the supplier of your choice: