TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
01 1Transo-Pharm USA LLC
02 1LGM Pharma
03 1Rochem International Inc
04 1Supriya Lifescience
05 1TAPI Technology & API Services
06 1Arihantanam Life Care
07 1Fuan Pharmaceutical
08 3GLAND PHARMA LIMITED
09 1Lewens Labs
10 1Mac-Chem Products (India) Pvt.Ltd
11 1Maithri Drugs
12 1Melody Healthcare Pvt Ltd
13 1Olon S.p.A
14 1Sailong Pharmaceutical
15 1Shenzhen Haorui
16 1Sumar Biotech
17 1Teva Pharmaceutical Industries
18 1Unimark Remedies Limited
19 2WUHAN ZY PHARMACEUTICAL CO LTD
20 1Zhejiang Hisun Pharmaceutical
21 1Blank
01 6China
02 11India
03 2Israel
04 1Italy
05 3U.S.A
06 1Blank
01 12Active
02 12Blank
01 3Valid
02 21Blank
01 24Blank
01 1WC-0170
02 1WC-0197
03 1WC-0227n
04 1WC-0399
05 1WC-0407
06 1WC-0427
07 18Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-07-21
Pay. Date : 2012-11-13
DMF Number : 22767
Submission : 2009-05-11
Status : Active
Type : II
Available Reg Filing : CA, ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-05-04
Pay. Date : 2022-04-20
DMF Number : 30422
Submission : 2016-03-31
Status : Active
Type : II
Date of Issue : 2020-09-09
Valid Till : 2023-06-28
Written Confirmation Number : WC-0407
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27696
Submission : 2013-11-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37231
Submission : 2022-06-15
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-08-18
Pay. Date : 2012-11-15
DMF Number : 26311
Submission : 2012-09-04
Status : Active
Type : II
NDC Package Code : 58623-0048
Start Marketing Date : 2018-01-18
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 : 26551
Submission : 2012-09-18
Status : Active
Type : II
Certificate Number : CEP 2018-056 - Rev 03
Issue Date : 2024-07-23
Type : Chemical
Substance Number : 2825
Status : Valid
Date of Issue : 2022-07-28
Valid Till : 2025-07-02
Written Confirmation Number : WC-0227n
Address of the Firm :
A Tigecycline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tigecycline, including repackagers and relabelers. The FDA regulates Tigecycline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tigecycline 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 Tigecycline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tigecycline supplier is an individual or a company that provides Tigecycline active pharmaceutical ingredient (API) or Tigecycline finished formulations upon request. The Tigecycline suppliers may include Tigecycline API manufacturers, exporters, distributors and traders.
click here to find a list of Tigecycline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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