Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Ltd
02 1Jai Radhe Sales
03 1Supriya Lifescience
04 1AANJANEYA LIFECARE LIMITED IN
05 1Arnold Suhr
06 1Arnold Suhr Qimpex Pte. Ltd. SG 048619 Singapore
07 1Buchler GmbH
08 1Inga Pharmaceuticals
09 1Micro Orgo Chem
10 1PT KIMIA FARMA PERSERO TBK
11 1PT Sinkona
12 1Prism Industries
13 1Roche Diagnostics GmbH
14 1SM Herbals Pvt Ltd
15 1Sibbiotech
16 1Vaishali Pharma Ltd
17 1Vital Laboratories Private Limited
01 2Germany
02 10India
03 2Indonesia
04 1Netherlands
05 1Russia
06 1Singapore
01 2Active
02 5Inactive
03 10Blank
01 1Valid
02 2Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
04 13Blank
01 17Blank
01 1WC-0006
02 1WC-0218
03 1WC-0527
04 14Blank
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Date of Issue : 2022-05-27
Valid Till : 2025-05-26
Written Confirmation Number : WC-0006
Address of the Firm :
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24063
Submission : 2010-07-19
Status : Active
Type : II
Certificate Number : R0-CEP 2005-117 - Rev 01
Issue Date : 2009-07-02
Type : Chemical
Substance Number : 19
Status : Withdrawn by EDQM F...
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-24
Pay. Date : 2013-06-14
DMF Number : 17086
Submission : 2004-01-05
Status : Active
Type : II
NDC Package Code : 12065-1704
Start Marketing Date : 1983-01-20
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 : 9462
Submission : 1991-12-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20951
Submission : 2007-09-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19905
Submission : 2006-10-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23415
Submission : 2009-12-15
Status : Inactive
Type : II
Certificate Number : R0-CEP 2009-387 - Rev 00
Issue Date : 2011-04-06
Type : Chemical
Substance Number : 19
Status : Withdrawn by EDQM F...
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31629
Submission : 2017-04-20
Status : Inactive
Type : II
A Quinine Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quinine Sulfate, including repackagers and relabelers. The FDA regulates Quinine Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quinine Sulfate 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 Quinine Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quinine Sulfate supplier is an individual or a company that provides Quinine Sulfate active pharmaceutical ingredient (API) or Quinine Sulfate finished formulations upon request. The Quinine Sulfate suppliers may include Quinine Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Quinine Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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