TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
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01 1Transo-Pharm USA LLC
02 1Rochem International Inc
03 1Transo-Pharm Handels GmbH
04 1Comhony Biotech
05 1Shanghai Minbiotech
06 1Chunghwa Chemical Synthesis & Biotech
07 1Omgene Life Sciences Pvt. Ltd
08 1Sumar Biotech
09 1Akums Lifesciences
10 1Aurobindo Pharma Limited
11 4BrightGene Bio-Medical Technology Co.,Ltd
12 1Concord Biotech
13 1Gnosis by Lesaffre
14 1Hubei Honch Pharmaceutical
15 1Huvepharma Italia S.r.l
16 1Livzon Group Fuzhou Fuxing Pharmaceutical Co., Ltd.
17 1Suzhou Biosyntech
18 1Xellia Pharmaceuticals ApS
19 1Yacht Bio-Technology
20 1Zhejiang Huida Biotech
21 1Blank
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01 11China
02 1Denmark
03 1France
04 1Germany
05 5India
06 1Italy
07 1Taiwan
08 2U.S.A
09 1Blank
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01 7Active
02 17Blank
01 24Blank
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01 24Blank
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01 24Blank
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01 24Blank
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01 142513-0017
02 152076-6279
03 184688-001
04 21Blank
01 24Blank
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6279
Start Marketing Date : 2023-09-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-07-01
Pay. Date : 2021-05-10
DMF Number : 35428
Submission : 2021-01-04
Status : Active
Type : II
NDC Package Code : 42513-0017
Start Marketing Date : 2021-01-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-04-23
Pay. Date : 2024-01-29
DMF Number : 39378
Submission : 2024-03-27
Status : Active
Type : II
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PharmaCompass offers a list of Dalbavancin 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 Dalbavancin manufacturer or Dalbavancin supplier for your needs.
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A Zeven manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zeven, including repackagers and relabelers. The FDA regulates Zeven manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zeven 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 Zeven supplier is an individual or a company that provides Zeven active pharmaceutical ingredient (API) or Zeven finished formulations upon request. The Zeven suppliers may include Zeven API manufacturers, exporters, distributors and traders.
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