Delivering high-quality, innovative solutions with regulatory excellence for the healthcare and chemical industries worldwide.
01 1Pramukh Pharmachem
02 1Inke S.A
03 2Dr. Reddy's Laboratories
04 1Emay Pharmaceuticals
05 1Jai Radhe Sales
06 1HRV Global Life Sciences
07 2TAPI Technology & API Services
08 1Anugraha Chemicals
09 1Aurobindo Pharma Limited
10 1Bazayan & Co
11 1CTX Lifesciences
12 1Cadila Pharmaceuticals
13 1Cambrex Corporation
14 1ChemSource
15 1Cipla
16 1Dr. Raju’s Pharma Solutions
17 1Fuan Pharmaceutical
18 1Gedeon Richter
19 1Hema Pharmaceuticals Pvt. Ltd
20 1Hermes Chemical
21 1Hikal
22 1Hikma Pharmaceuticals
23 1Ipca Laboratories
24 1Maps Laboratories Private Limited
25 1NINGBO TEAM PHARMACEUTICAL CO., LTD. CN 315 201 Ningbo
26 2Natco Pharma
27 1Nishchem International Pvt. Ltd
28 1Qilu Pharmaceutical
29 1Rampex Labs
30 1SMS Pharmaceuticals
31 1ScinoPharm Taiwan, Ltd
32 1Shodhana Laboratories Pvt. Ltd
33 1Shouyuan Chemical
34 1Sun Pharmaceutical Industries Limited
35 1Suvan Lifesciences
36 1Symed Labs
37 1Taro Pharmaceutical Industries
38 1Teva Pharmaceutical Industries
39 1Therapiva
01 4China
02 1Hungary
03 27India
04 3Israel
05 1Spain
06 1Taiwan
07 4U.S.A
08 1United Kingdom
01 17Active
02 3Inactive
03 22Blank
01 2Expired
02 16Valid
03 24Blank
01 1219MF10022
02 1219MF10374
03 1221MF10130
04 1302MF10019
05 1306MF10103
06 37Blank
01 1WC-0014
02 1WC-0026
03 1WC-0043Amended
04 1WC-0071
05 1WC-0074
06 1WC-0091
07 1WC-0094nA2A
08 1WC-0097
09 1WC-0144nA2
10 1WC-0168
11 1WC-0230
12 1WC-0331
13 1WC-0382A4
14 29Blank
Delivering high-quality, innovative solutions with regulatory excellence for the healthcare and chemical industries worldwide.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16317
Submission : 2002-12-13
Status : Active
Type : II
Certificate Number : R1-CEP 2005-056 - Rev 00
Issue Date : 2012-05-24
Type : Chemical
Substance Number : 2016
Status : Valid
NDC Package Code : 64567-0005
Start Marketing Date : 2009-08-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-09-23
Pay. Date : 2015-09-09
DMF Number : 15436
Submission : 2001-05-15
Status : Active
Type : II
Certificate Number : R1-CEP 2005-071 - Rev 06
Issue Date : 2023-05-23
Type : Chemical
Substance Number : 2016
Status : Valid
Registration Number : 302MF10019
Registrant's Address : 8-2-337, Road No. 3,Banjara Hills,Hyderabad 500 034,TELANGANA,INDIA
Initial Date of Registration : 2020-01-31
Latest Date of Registration :
Date of Issue : 2022-06-08
Valid Till : 2025-06-04
Written Confirmation Number : WC-0043Amended
Address of the Firm :
NDC Package Code : 55111-017
Start Marketing Date : 2010-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : BR, ASMF, CA |
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15642
Submission : 2001-10-01
Status : Active
Type : II
Registration Number : 219MF10022
Registrant's Address : 13 Pallagi u(´)t, Debrecen, 4042-Hungary
Initial Date of Registration : 2007-01-22
Latest Date of Registration :
Available Reg Filing : ASMF |
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 221MF10130
Registrant's Address : 8-2-337, Road No. 3,Banjara Hills,Hyderabad 500 034,TELANGANA,INDIA
Initial Date of Registration : 2009-06-30
Latest Date of Registration :
NDC Package Code : 55111-017
Start Marketing Date : 2010-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : BR, ASMF, CA |
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17053
Submission : 2003-12-22
Status : Inactive
Type : II
Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-12-21
Pay. Date : 2022-12-19
DMF Number : 22181
Submission : 2008-11-13
Status : Active
Type : II
Certificate Number : R0-CEP 2017-185 - Rev 00
Issue Date : 2018-08-17
Type : Chemical
Substance Number : 2016
Status : Expired
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-08-28
Pay. Date : 2013-08-19
DMF Number : 22340
Submission : 2008-12-23
Status : Active
Type : II
Certificate Number : R1-CEP 2009-319 - Rev 04
Issue Date : 2019-09-16
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2019-06-26
Valid Till : 2022-07-02
Written Confirmation Number : WC-0071
Address of the Firm :
NDC Package Code : 67835-5014
Start Marketing Date : 2009-05-13
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 : 17034
Submission : 2003-12-16
Status : Active
Type : II
Certificate Number : R1-CEP 2008-174 - Rev 04
Issue Date : 2023-02-01
Type : Chemical
Substance Number : 2016
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-10-23
Pay. Date : 2018-09-13
DMF Number : 15752
Submission : 2001-12-05
Status : Active
Type : II
Certificate Number : R1-CEP 2003-130 - Rev 01
Issue Date : 2011-12-12
Type : Chemical
Substance Number : 2016
Status : Valid
Registration Number : 219MF10374
Registrant's Address : 1205 11th Street, Charles City, Iowa, U.S. S. A.
Initial Date of Registration : 2007-12-19
Latest Date of Registration :
NDC Package Code : 59116-1850
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2013-03-13
Registration Number : 20130313-47-B-343-17
Manufacturer Name : Cambrex Charles City, Inc
Manufacturer Address : 1205 11th st. Charles City, IA 50616, USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16786
Submission : 2003-09-04
Status : Active
Type : II
Certificate Number : R1-CEP 2004-209 - Rev 03
Issue Date : 2020-03-04
Type : Chemical
Substance Number : 2016
Status : Valid
Registration Number : 306MF10103
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2024-07-17
Latest Date of Registration :
Date of Issue : 2022-09-01
Valid Till : 2025-07-02
Written Confirmation Number : WC-0074
Address of the Firm :
NDC Package Code : 65691-0035
Start Marketing Date : 2003-09-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-02-25
Pay. Date : 2020-02-20
DMF Number : 15990
Submission : 2002-05-27
Status : Active
Type : II
NDC Package Code : 65129-2161
Start Marketing Date : 2001-07-31
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 : 16976
Submission : 2003-11-25
Status : Active
Type : II
Certificate Number : R0-CEP 2009-191 - Rev 02
Issue Date : 2014-03-31
Type : Chemical
Substance Number : 2016
Status : Expired
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18180
Submission : 2005-02-25
Status : Active
Type : II
Certificate Number : CEP 2003-221 - Rev 05
Issue Date : 2023-10-03
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0014
Address of the Firm :
NDC Package Code : 63850-2706
Start Marketing Date : 2016-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-01-14
Pay. Date : 2014-01-08
DMF Number : 20675
Submission : 2007-07-12
Status : Active
Type : II
NDC Package Code : 63850-2706
Start Marketing Date : 2016-01-12
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 : 16562
Submission : 2003-04-23
Status : Active
Type : II
Certificate Number : R1-CEP 2004-066 - Rev 04
Issue Date : 2022-08-17
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-01-08
Pay. Date : 2015-01-02
DMF Number : 19071
Submission : 2005-12-19
Status : Active
Type : II
Certificate Number : CEP 2007-012 - Rev 06
Issue Date : 2024-02-28
Type : Chemical
Substance Number : 2016
Status : Valid
NDC Package Code : 65862-377
Start Marketing Date : 2023-11-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-04
Pay. Date : 2013-08-21
DMF Number : 20771
Submission : 2007-08-20
Status : Active
Type : II
Certificate Number : R1-CEP 2007-237 - Rev 02
Issue Date : 2019-09-18
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091
Address of the Firm :
NDC Package Code : 57451-1153
Start Marketing Date : 2019-11-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea United Pharmaceutical Co., Ltd.
Registration Date : 2013-12-27
Registration Number : 20100226-47-B-298-13(1)
Manufacturer Name : IPCA Laboratories Limited
Manufacturer Address : PO Sejavta, District-Ratlam (MP) 457001, India
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15724
Submission : 2001-11-15
Status : Active
Type : II
Certificate Number : R1-CEP 2006-279 - Rev 03
Issue Date : 2014-07-28
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-09-08
Written Confirmation Number : WC-0144nA2
Address of the Firm :
NDC Package Code : 53104-7540
Start Marketing Date : 2018-11-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15783
Submission : 2001-12-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23330
Submission : 2009-11-25
Status : Inactive
Type : II
Date of Issue : 2022-04-04
Valid Till : 2025-01-13
Written Confirmation Number : WC-0331
Address of the Firm :
Certificate Number : R1-CEP 2003-053 - Rev 01
Issue Date : 2011-08-22
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2022-06-24
Valid Till : 2025-07-02
Written Confirmation Number : WC-0097
Address of the Firm :
Certificate Number : R1-CEP 2009-114 - Rev 01
Issue Date : 2023-05-04
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2019-10-10
Valid Till : 2022-07-02
Written Confirmation Number : WC-0230
Address of the Firm :
Certificate Number : R1-CEP 2004-042 - Rev 03
Issue Date : 2021-11-23
Type : Chemical
Substance Number : 2016
Status : Valid
NDC Package Code : 51846-1025
Start Marketing Date : 2017-11-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R0-CEP 2019-252 - Rev 00
Issue Date : 2021-12-06
Type : Chemical
Substance Number : 2016
Status : Valid
Date of Issue : 2021-06-22
Valid Till : 2022-08-08
Written Confirmation Number : WC-0382A4
Address of the Firm :
NDC Package Code : 66022-0204
Start Marketing Date : 1992-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ondansetron Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ondansetron Hydrochloride, including repackagers and relabelers. The FDA regulates Ondansetron Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ondansetron Hydrochloride 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 Ondansetron Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ondansetron Hydrochloride supplier is an individual or a company that provides Ondansetron Hydrochloride active pharmaceutical ingredient (API) or Ondansetron Hydrochloride finished formulations upon request. The Ondansetron Hydrochloride suppliers may include Ondansetron Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ondansetron Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 39 companies offering Ondansetron Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?