TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
01 1Transo-Pharm USA LLC
02 2TAPI Technology & API Services
03 1Asia Pioneer Pharmaceuticals
04 1Aurobindo Pharma Limited
05 1Beijing Lunarsun Pharmaceutical Co., Ltd
06 1Chongqing Shenghuaxi Pharma. Co., Ltd
07 1CordenPharma
08 5Curia
09 1FangYuan Pharmaceutical
10 2Fuan Pharmaceutical
11 1Globofarm International
12 1Hainan Haiyao
13 1Hanways Chempharm
14 1Orchid Pharma
15 1Teva Pharmaceutical Industries
01 7China
02 1Germany
03 3India
04 3Israel
05 7U.S.A
01 9Active
02 4Inactive
03 8Blank
01 21Blank
01 1219MF10225
02 20Blank
01 21Blank
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16751
Submission : 2003-08-08
Status : Inactive
Type : II
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 : 2012-12-24
Pay. Date : 2012-12-03
DMF Number : 19342
Submission : 2006-04-11
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-28
Pay. Date : 2013-09-30
DMF Number : 27508
Submission : 2013-09-11
Status : Active
Type : II
NDC Package Code : 52952-001
Start Marketing Date : 2012-07-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-09-12
Pay. Date : 2023-07-31
DMF Number : 38649
Submission : 2023-07-31
Status : Active
Type : II
NDC Package Code : 59651-859
Start Marketing Date : 2024-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-07-15
Pay. Date : 2013-10-30
DMF Number : 26856
Submission : 2013-10-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17184
Submission : 2004-02-23
Status : Active
Type : II
NDC Package Code : 13538-001
Start Marketing Date : 2009-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (200kg/200kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-07-09
Pay. Date : 2019-05-17
DMF Number : 33731
Submission : 2019-04-05
Status : Active
Type : II
NDC Package Code : 13538-001
Start Marketing Date : 2009-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (200kg/200kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-08-13
Pay. Date : 2019-06-03
DMF Number : 33762
Submission : 2019-04-09
Status : Active
Type : II
NDC Package Code : 13538-001
Start Marketing Date : 2009-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (200kg/200kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38055
Submission : 2023-05-12
Status : Active
Type : II
NDC Package Code : 13538-001
Start Marketing Date : 2009-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (200kg/200kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39731
Submission : 2024-05-21
Status : Active
Type : II
NDC Package Code : 13538-001
Start Marketing Date : 2009-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (200kg/200kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23971
Submission : 2010-07-06
Status : Inactive
Type : II
NDC Package Code : 52952-001
Start Marketing Date : 2012-07-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20014
Submission : 2006-12-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20907
Submission : 2007-09-07
Status : Inactive
Type : II
Registration Number : 219MF10225
Registrant's Address : VIA MURILLO, 7, 04013-SERMONETA (LATINA), ITALY
Initial Date of Registration : 2007-07-06
Latest Date of Registration : --
A Aztreonam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aztreonam, including repackagers and relabelers. The FDA regulates Aztreonam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aztreonam 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 Aztreonam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aztreonam supplier is an individual or a company that provides Aztreonam active pharmaceutical ingredient (API) or Aztreonam finished formulations upon request. The Aztreonam suppliers may include Aztreonam API manufacturers, exporters, distributors and traders.
click here to find a list of Aztreonam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 15 companies offering Aztreonam
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?