Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.

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01 1Alchem International Private Ltd
02 2Alkaloids Bioactives Private Limited
03 1Phytex Australia
04 1Zeon Pharma Industries India Pvt Ltd
05 1Sanofi
06 1LGM Pharma
07 1DKSH
08 1Jai Radhe Sales
09 1Tenatra Exports
10 1Honour Lab Limited
11 1Chemical Resources
12 1Dr. Willmar Schwabe Extracta
13 1Ennature Biopharma
14 1Harman Finochem
15 1Hindustan Herbals Limited
16 3Indena
17 1India Glycols
18 1Inga Pharmaceuticals
19 1Jin Dun Medical
20 1Johannes Burger Bau
21 1Par Pharmaceutical
22 1Pcca
23 1Quad Lifesciences
24 1Remedy Labs
25 1Sanmar Speciality Chemicals Limited IN 600 086 Chennai
26 1Sarv Biolabs Pvt Ltd
27 1Solara Active Pharma Sciences
28 1Varion Lifesciences
29 1Vital Laboratories Private Limited
30 1elm-plastic GmbH
31 1Blank
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01 1Australia
02 1China
03 1Denmark
04 1France
05 2Germany
06 20India
07 3Italy
08 1Switzerland
09 2U.S.A
10 1United Kingdom
11 1Blank
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01 10Active
02 5Inactive
03 19Blank
01 7Valid
02 2Withdrawn by EDQM Failure to CEP procedure
03 25Blank
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01 1218MF10226
02 33Blank
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01 1WC-0006
02 1WC-0192
03 1WC-0294
04 1WC-0299
05 1WC-0300
06 1WC-0322
07 1WC-0362
08 1WC-0450
09 26Blank
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01 34Blank
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01 117359-5000
02 151927-0277
03 155742-127
04 166064-1008
05 168404-0001
06 169037-0011
07 170054-002
08 185973-0001
09 26Blank
01 34Blank
Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22564
Submission : 2009-02-18
Status : Active
Type : II
Certificate Number : CEP 2019-146 - Rev 02
Issue Date : 2025-05-21
Type : Chemical
Substance Number : 758
Status : Valid
Date of Issue : 2025-06-27
Valid Till : 2028-05-26
Written Confirmation Number : WC-0006
Address of the Firm :
NDC Package Code : 55742-127
Start Marketing Date : 2016-12-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : CH |
Alkaloids Bioactives: US FDA, TGA & ISO-Certified Pioneers in Plant-Derived APIs, Nutraceuticals & Cosmeceuticals
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-07-24
Pay. Date : 2020-07-16
DMF Number : 24155
Submission : 2010-09-09
Status : Active
Type : II
Date of Issue : 2022-11-25
Valid Till : 2025-07-02
Written Confirmation Number : WC-0192
Address of the Firm :
NDC Package Code : 85973-0001
Start Marketing Date : 2017-11-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Experts in producing high-quality APIs from natural sources, specializing in advanced extraction and isolation techniques.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5163
Submission : 1983-12-01
Status : Inactive
Type : II
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-02-18
Pay. Date : 2015-05-26
DMF Number : 29401
Submission : 2015-06-05
Status : Active
Type : II
Date of Issue : 2025-09-03
Valid Till : 2028-09-02
Written Confirmation Number : WC-0362
Address of the Firm :
NDC Package Code : 69037-0011
Start Marketing Date : 2009-07-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : CN |
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PharmaCompass offers a list of Colchicine 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 Colchicine manufacturer or Colchicine supplier for your needs.
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A Tox21_300582 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300582, including repackagers and relabelers. The FDA regulates Tox21_300582 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300582 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 Tox21_300582 supplier is an individual or a company that provides Tox21_300582 active pharmaceutical ingredient (API) or Tox21_300582 finished formulations upon request. The Tox21_300582 suppliers may include Tox21_300582 API manufacturers, exporters, distributors and traders.
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We have 30 companies offering Tox21_300582
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