Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
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01 1Aarti Pharmalabs
02 1Inke S.A
03 1Medichem S.A
04 2Neuland Laboratories
05 1Tenatra Chemie
06 1Zeon Pharma Industries India Pvt Ltd
07 1Farmhispania
08 1Apotex Pharmachem
09 1CHEMO
10 1Changzhou Pharmaceutical Factory
11 1ChemSource
12 1DEAFARMA
13 1Esteve Quimica
14 1GULF OIL Corporation Limited IN 500 018 Hyderabad
15 1Gedeon Richter
16 1Hangzhou Think Chemical Co.Ltd
17 1Hengdian Group
18 1Jin Dun Medical
19 1Kongo Chemical Co., Ltd.
20 2Krka
21 1Lek Pharmaceuticals
22 2Maprimed
23 1Merck & Co
24 1Nosch Labs Pvt
25 1Ohara Pharmaceutical
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27 1Ramdev Chemicals Pvt Ltd
28 2Sri Krishna Pharmaceuticals
29 1Srini Pharmaceuticals
30 1Sun Pharmaceutical Industries Limited
31 1Wockhardt
32 1Zhejiang Changming Pharmaceuticals
33 1Zhejiang Huahai Pharmaceutical
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01 2Argentina
02 1Canada
03 7China
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05 13India
06 1Italy
07 2Japan
08 3Slovenia
09 5Spain
10 2U.S.A
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01 5Active
02 12Inactive
03 20Blank
01 1Expired
02 9Valid
03 1Withdrawn by EDQM Failure to CEP procedure
04 3Withdrawn by Holder
05 23Blank
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01 1217MF11207
02 1219MF10252
03 1220MF10175
04 1227MF10268
05 33Blank
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01 1WC-0027
02 1WC-0033
03 1WC-0036
04 1WC-0037
05 1WC-0128
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Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2000-070 - Rev 04
Issue Date : 2019-02-21
Type : Chemical
Substance Number : 1420
Status : Valid
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-12-B-49-06
Manufacturer Name : Inke, SA (Group Vita)
Manufacturer Address : Area Industrial del Llobregat, C/Argent 1, 08755 Castellbisbal Barcelona
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13055
Submission : 1998-06-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15434
Submission : 2001-05-15
Status : Active
Type : II
Certificate Number : CEP 2024-245 - Rev 00
Issue Date : 2024-11-13
Type : Chemical
Substance Number : 1420
Status : Valid
Registration Number : 219MF10252
Registrant's Address : 11th Floor (5th Office Level), Phoenix IVY Building, Plot No. 573A-Ⅲ, Road No. 82, Jubilee Hills,Hyderabad-33 Telangana, India
Initial Date of Registration : 2007-07-26
Latest Date of Registration :
Date of Issue : 2022-07-28
Valid Till : 2025-06-16
Written Confirmation Number : WC-0036
Address of the Firm :
NDC Package Code : 58032-0125
Start Marketing Date : 2017-11-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2018-10-14
Registration Number : 20050831-12-B-44-02(1)
Manufacturer Name : Neuland Lab. Ltd
Manufacturer Address : Sy.No: 347,473,474,490/2 Bonthapalli (V), Veerabhadraswamy temple road, Jinnaram (M), Medak (Dist.)-502 313 Telangana, India
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11525
Submission : 1995-05-19
Status : Active
Type : II
Certificate Number : R1-CEP 2006-104 - Rev 01
Issue Date : 2013-03-14
Type : Chemical
Substance Number : 1420
Status : Valid
NDC Package Code : 17404-0009
Start Marketing Date : 2000-02-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-06-28
Pay. Date : 2016-06-16
DMF Number : 19984
Submission : 2006-11-17
Status : Active
Type : II
Certificate Number : R1-CEP 2003-078 - Rev 14
Issue Date : 2023-06-07
Type : Chemical
Substance Number : 1420
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-06-16
Written Confirmation Number : WC-0037
Address of the Firm :
NDC Package Code : 58032-0125
Start Marketing Date : 2017-11-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2018-10-14
Registration Number : 20050831-12-B-44-02(1)
Manufacturer Name : Neuland Lab. Ltd
Manufacturer Address : Sy.No: 347,473,474,490/2 Bonthapalli (V), Veerabhadraswamy temple road, Jinnaram (M), Medak (Dist.)-502 313 Telangana, India
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12939
Submission : 1998-04-08
Status : Inactive
Type : II
Certificate Number : R1-CEP 2001-408 - Rev 03
Issue Date : 2010-11-25
Type : Chemical
Substance Number : 1420
Status : Withdrawn by Holder
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11866
Submission : 1996-02-27
Status : Inactive
Type : II
Certificate Number : R1-CEP 2000-258 - Rev 04
Issue Date : 2020-10-28
Type : Chemical
Substance Number : 1420
Status : Withdrawn by Holder
58
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A Kinfil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kinfil, including repackagers and relabelers. The FDA regulates Kinfil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kinfil 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 Kinfil supplier is an individual or a company that provides Kinfil active pharmaceutical ingredient (API) or Kinfil finished formulations upon request. The Kinfil suppliers may include Kinfil API manufacturers, exporters, distributors and traders.
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