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01 1Axplora
02 1LGM Pharma
03 1Apicore
04 1Archimica
05 1Ash Stevens
06 1ChemPacific Corp
07 2Emcure Pharmaceuticals
08 1Fareva
09 1Fresenius Kabi AB Brunna
10 1Fresenius Kabi Oncology Limited
11 1Hetero Drugs
12 1Kekule Pharma
13 2Natco Pharma
14 1Sakar Healthcare
15 1Shilpa Medicare
16 1Shivalik Rasayan
17 1Vannsh Life Sciences
18 1Viatris
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01 1Germany
02 12India
03 1Italy
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06 4U.S.A
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01 7Active
02 3Inactive
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01 6Valid
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01 1230MF10027
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01 1WC-0041
02 1WC-0115
03 1WC-0147
04 1WC-0226
05 1WC-0372
06 1WC-0372(1)
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01 120180726-210-J-248
02 120220608-210-J-1307
03 120220926-210-J-1369
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01 114096-147
02 114593-865
03 146014-1116
04 146439-8734
05 148957-0010
06 182920-008
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GDUFA
DMF Review : Reviewed
Rev. Date : 2013-08-08
Pay. Date : 2012-12-17
DMF Number : 25933
Submission : 2012-03-27
Status : Active
Type : II
NDC Package Code : 46439-8734
Start Marketing Date : 2011-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Pharma Science Korea Co., Ltd.
Registration Date : 2022-06-08
Registration Number : 20220608-210-J-1307
Manufacturer Name : Farmabios SpA
Manufacturer Address : Via Pavia 1, Gropello Cairoli, 27027, Italy
Available Reg Filing : SAU |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-25
Pay. Date : 2012-11-21
DMF Number : 25667
Submission : 2012-02-02
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-06-10
Pay. Date : 2015-05-27
DMF Number : 23924
Submission : 2010-08-05
Status : Active
Type : II
Certificate Number : R1-CEP 2016-270 - Rev 00
Issue Date : 2023-05-17
Type : Chemical
Substance Number : 542
Status : Valid
NDC Package Code : 14096-147
Start Marketing Date : 2011-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Product Not Available For Sales
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-09-03
Pay. Date : 2014-07-10
DMF Number : 27006
Submission : 2013-06-06
Status : Active
Type : II
Certificate Number : R1-CEP 2013-212 - Rev 00
Issue Date : 2020-04-28
Type : Chemical
Substance Number : 542
Status : Valid
NDC Package Code : 46014-1116
Start Marketing Date : 2014-06-02
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 : 21126
Submission : 2007-12-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25393
Submission : 2011-10-18
Status : Inactive
Type : II
Date of Issue : 2019-10-07
Valid Till : 2022-06-12
Written Confirmation Number : WC-0372
Address of the Firm :
Certificate Number : CEP 2010-374 - Rev 08
Issue Date : 2025-02-03
Type : Chemical
Substance Number : 542
Status : Valid
Date of Issue : 2019-07-08
Valid Till : 2022-07-07
Written Confirmation Number : WC-0115
Address of the Firm :
Certificate Number : R0-CEP 2021-356 - Rev 00
Issue Date : 2022-12-01
Type : Chemical
Substance Number : 542
Status : Valid
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PharmaCompass offers a list of Busulfan 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 Busulfan manufacturer or Busulfan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Busulfan manufacturer or Busulfan supplier.
PharmaCompass also assists you with knowing the Busulfan API Price utilized in the formulation of products. Busulfan API Price is not always fixed or binding as the Busulfan Price is obtained through a variety of data sources. The Busulfan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Busulfan (Myleran, Busulfex) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Busulfan (Myleran, Busulfex), including repackagers and relabelers. The FDA regulates Busulfan (Myleran, Busulfex) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Busulfan (Myleran, Busulfex) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Busulfan (Myleran, Busulfex) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Busulfan (Myleran, Busulfex) supplier is an individual or a company that provides Busulfan (Myleran, Busulfex) active pharmaceutical ingredient (API) or Busulfan (Myleran, Busulfex) finished formulations upon request. The Busulfan (Myleran, Busulfex) suppliers may include Busulfan (Myleran, Busulfex) API manufacturers, exporters, distributors and traders.
click here to find a list of Busulfan (Myleran, Busulfex) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 18 companies offering Busulfan (Myleran, Busulfex)
Get in contact with the supplier of your choice: