Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
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01 3Alchem International Private Ltd
02 1Zeon Pharma Industries India Pvt Ltd
03 1Pharm-RX Chemical
04 2ALPS Pharmaceutical Ind. Co. Ltd.
05 1Beloorbayir Biotech
06 1Chemical Resources
07 1Finzelberg GmbH & Co. KG
08 1Inga Pharmaceuticals
09 1Kothari Phytochemicals & Industries
10 1Santen Pharmaceutical
11 1Shashi Phytochemical Industries
12 1Vital Laboratories Private Limited
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01 1Germany
02 10India
03 3Japan
04 1U.S.A
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01 2Active
02 3Inactive
03 10Blank
01 15Blank
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01 1218MF10620
02 1219MF10246
03 1225MF10137
04 1227MF10003
05 11Blank
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01 1WC-0300
02 1WC-0350
03 13Blank
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 227MF10003
Registrant's Address : 201,Empire Plaza,Mehrauli-Gurgaon Road Sultanpur,New Delhi-110 030,INDIA
Initial Date of Registration : 2015-01-05
Latest Date of Registration :
NDC Package Code : 55742-007
Start Marketing Date : 2012-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 225MF10137
Registrant's Address : 201,Empire Plaza,Mehrauli-Gurgaon Road Sultanpur,New Delhi-110 030,INDIA
Initial Date of Registration : 2013-07-23
Latest Date of Registration :
NDC Package Code : 55742-007
Start Marketing Date : 2012-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 219MF10246
Registrant's Address : 301,Avalon Apartments,Mehrauli-Gurgaon Road Manglapuri,New Delhi-110 030,INDIA
Initial Date of Registration : 2007-07-17
Latest Date of Registration :
NDC Package Code : 55742-007
Start Marketing Date : 2012-05-31
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 : 32164
Submission : 2017-11-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32508
Submission : 2018-01-29
Status : Active
Type : II
NDC Package Code : 52537-001
Start Marketing Date : 2012-12-19
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 : 29523
Submission : 2015-06-11
Status : Inactive
Type : II
Date of Issue : 2022-01-04
Valid Till : 2025-02-01
Written Confirmation Number : WC-0350
Address of the Firm :
NDC Package Code : 55977-100
Start Marketing Date : 1996-10-01
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 : 13991
Submission : 1999-02-23
Status : Inactive
Type : II
NDC Package Code : 17353-0902
Start Marketing Date : 2013-09-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14132
Submission : 1999-05-01
Status : Inactive
Type : II
NDC Package Code : 17353-0902
Start Marketing Date : 2013-09-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
Date of Issue : 2024-05-20
Valid Till : 2027-01-08
Written Confirmation Number : WC-0300
Address of the Firm :
Registration Number : 218MF10620
Registrant's Address : Niityhaankatu 20, FI-33720 Tampere, Finland
Initial Date of Registration : 2006-07-03
Latest Date of Registration :
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A Sennosides manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sennosides, including repackagers and relabelers. The FDA regulates Sennosides manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sennosides 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 Sennosides supplier is an individual or a company that provides Sennosides active pharmaceutical ingredient (API) or Sennosides finished formulations upon request. The Sennosides suppliers may include Sennosides API manufacturers, exporters, distributors and traders.
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We have 12 companies offering Sennosides
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