Chirogate is a professional Prostaglandin manufacturer.

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01 3Chirogate International
02 1Nuray Chemicals Private Limited
03 1EUROAPI
04 1LGM Pharma
05 1ChemWerth Inc
06 1Dr. Reddy's Laboratories
07 1HRV Pharma
08 1Alphora Research
09 1Emcure Pharmaceuticals
10 1Eurofins CDMO
11 5MSN Laboratories
12 1Mannkind
13 2Mehta API
14 1Pfizer Inc
15 1TIEN (Tianjin) Pharmaceutical
16 1Turtle Pharma
17 1Yonsung Fine Chemicals
18 1Zhejiang Ausun Pharmaceutical
19 2Blank
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01 1Canada
02 2China
03 2France
04 12India
05 1South Korea
06 3Taiwan
07 4U.S.A
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01 13Active
02 1Inactive
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01 2WC-0214
02 1WC-0226
03 1WC-0416
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01 120250417-210-J-1862
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01 114501-0015
02 114501-0016
03 114501-0017
04 140016-009
05 143076-001
06 154893-0022
07 154893-0024
08 168245-0008
09 168245-0009
10 182231-115
11 183511-033
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28340
Submission : 2016-08-15
Status : Active
Type : II
NDC Package Code : 68245-0008
Start Marketing Date : 2010-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-02-16
Pay. Date : 2016-09-20
DMF Number : 30861
Submission : 2016-09-27
Status : Active
Type : II
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-05-23
Pay. Date : 2016-11-25
DMF Number : 31145
Submission : 2016-12-09
Status : Active
Type : II
NDC Package Code : 82231-115
Start Marketing Date : 2019-11-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-01-06
Pay. Date : 2014-07-15
DMF Number : 28458
Submission : 2014-09-16
Status : Active
Type : II
NDC Package Code : 68245-0009
Start Marketing Date : 2010-01-01
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 : 29207
Submission : 2015-08-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33169
Submission : 2018-10-17
Status : Active
Type : II

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PharmaCompass offers a list of Treprostinil Sodium 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 Treprostinil Sodium manufacturer or Treprostinil Sodium supplier for your needs.
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A Remodulin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Remodulin, including repackagers and relabelers. The FDA regulates Remodulin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Remodulin 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 Remodulin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Remodulin supplier is an individual or a company that provides Remodulin active pharmaceutical ingredient (API) or Remodulin finished formulations upon request. The Remodulin suppliers may include Remodulin API manufacturers, exporters, distributors and traders.
click here to find a list of Remodulin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 18 companies offering Remodulin
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