LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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01 1LGM Pharma
02 2Veranova
03 2Rusan Pharma
04 1Arevipharma
05 2Cambrex Corporation
06 1Grindeks AS
07 2Hameln rds
08 1Jiangsu Nhwa Pharmaceutical
09 1Johnson & Johnson Innovative Medicine
10 2Kern Pharma S.L.
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07 2Slovakia
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09 8U.S.A
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01 5Active
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01 7Valid
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01 120220421-210-J-1273
02 120220421-210-J-1273(A)
03 120220518-210-J-1301
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01 10406-0310
02 10406-0330
03 10406-0672
04 10406-0678
05 138779-1968
06 149812-0021
07 151927-3213
08 182393-121
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9399
Submission : 1991-10-31
Status : Active
Type : II
Certificate Number : R1-CEP 2005-162 - Rev 02
Issue Date : 2014-10-14
Type : Chemical
Substance Number : 1269
Status : Valid
NDC Package Code : 49812-0021
Start Marketing Date : 1995-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Samung Industry Co., Ltd.
Registration Date : 2022-04-25
Registration Number : 20220421-210-J-1273(A)
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Certificate Number : R1-CEP 2005-149 - Rev 01
Issue Date : 2013-02-20
Type : Chemical
Substance Number : 1569
Status : Withdrawn by Holder
Registrant Name : Baeksu Pharmaceutical Co., Ltd.
Registration Date : 2022-04-21
Registration Number : 20220421-210-J-1273
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12183
Submission : 1996-10-21
Status : Active
Type : II
Certificate Number : CEP 2019-054 - Rev 01
Issue Date : 2026-02-05
Type : Chemical
Substance Number : 1569
Status : Valid
NDC Package Code : 0406-0678
Start Marketing Date : 2017-01-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registrant Name : Nosa Chemical Co., Ltd.
Registration Date : 2022-05-18
Registration Number : 20220518-210-J-1301
Manufacturer Name : SpecGx LLC
Manufacturer Address : 3600 North 2nd Street, St. Louis, MO 63147, USA

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14505
Submission : 1999-10-27
Status : Active
Type : II
Certificate Number : CEP 2017-095 - Rev 01
Issue Date : 2024-05-06
Type : Chemical
Substance Number : 1269
Status : Valid
NDC Package Code : 0406-0310
Start Marketing Date : 2013-04-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30985
Submission : 2016-12-19
Status : Active
Type : II
NDC Package Code : 0406-0330
Start Marketing Date : 2013-04-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30986
Submission : 2017-08-23
Status : Active
Type : II
NDC Package Code : 0406-0672
Start Marketing Date : 2013-04-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11327
Submission : 1995-02-06
Status : Inactive
Type : II
Certificate Number : R1-CEP 1998-116 - Rev 07
Issue Date : 2022-07-07
Type : Chemical
Substance Number : 1269
Status : Valid

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PharmaCompass offers a list of Sufentanil Citrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Sufentanil Citrate manufacturer or Sufentanil Citrate supplier for your needs.
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A Sufentanil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sufentanil, including repackagers and relabelers. The FDA regulates Sufentanil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sufentanil 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 Sufentanil supplier is an individual or a company that provides Sufentanil active pharmaceutical ingredient (API) or Sufentanil finished formulations upon request. The Sufentanil suppliers may include Sufentanil API manufacturers, exporters, distributors and traders.
click here to find a list of Sufentanil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
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