LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 1LGM Pharma
02 2Dr. Reddy's Laboratories
03 1Jai Radhe Sales
04 2Moehs Iberica
05 1Faran Shimi Pharmaceutical
06 1Vamsi Labs
07 1HRV Global Life Sciences
08 1Zeon Pharma Industries India Pvt Ltd
09 1Apotex Pharmachem
10 1Aspire Lifesciences Pvt Ltd
11 1Asymchem Laboratories
12 2Aurobindo Pharma Limited
13 1CHEMO
14 1Cerata Pharmaceuticals
15 2Chromo Laboratories
16 1Cipla
17 1Darou Pakhsh Pharma Chem
18 2Divis Laboratories
19 1Hovione
20 1Ipca Laboratories
21 1KOLON Life Science, Inc
22 2MSN Laboratories
23 1Maithili Life Sciences
24 3Natco Pharma
25 1Nosch Labs Pvt
26 1Orchid Pharma
27 1Phalanx Labs
28 2Quimica Sintetica
29 1SM BIOMED
30 4SMS Pharmaceuticals
31 1Shandong Xinhua Pharmaceutical
32 1Smilax Laboratories Limited
33 1Srini Pharmaceuticals
34 1Sun Pharmaceutical Industries Limited
35 2Synergene Active Ingredients Pvt Ltd
36 1Therapiva
37 1Tianish Laboratories
38 1Viatris
01 1Canada
02 2China
03 36India
04 2Iran
05 1Malaysia
06 1Portugal
07 1South Korea
08 5Spain
09 2U.S.A
01 18Active
02 8Inactive
03 25Blank
01 9Valid
02 5Withdrawn by Holder
03 37Blank
01 1221MF10241
02 1223MF10048
03 1223MF10060
04 1228MF10195
05 47Blank
01 1WC-0017
02 1WC-0022
03 1WC-0026
04 1WC-0027
05 2WC-0030
06 1WC-0071
07 1WC-0118
08 1WC-0168
09 1WC-0317
10 1WC-0317A2
11 1WC-0347
12 1WC-0465
13 38Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16534
Submission : 2003-03-21
Status : Active
Type : II
Certificate Number : CEP 2023-022 - Rev 00
Issue Date : 2023-10-30
Type : Chemical
Substance Number : 1573
Status : Valid
NDC Package Code : 55111-060
Start Marketing Date : 2003-03-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-24
Pay. Date : 2013-06-19
DMF Number : 17352
Submission : 2004-04-29
Status : Active
Type : II
NDC Package Code : 52932-0727
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF |
Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-12-17
Pay. Date : 2024-11-21
DMF Number : 37551
Submission : 2022-09-30
Status : Active
Type : II
NDC Package Code : 55111-060
Start Marketing Date : 2003-03-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-11-22
Pay. Date : 2013-02-13
DMF Number : 24026
Submission : 2010-08-02
Status : Active
Type : II
NDC Package Code : 52932-0727
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-16
Pay. Date : 2014-04-30
DMF Number : 16930
Submission : 2003-10-23
Status : Active
Type : II
Certificate Number : R1-CEP 2003-245 - Rev 03
Issue Date : 2017-02-14
Type : Chemical
Substance Number : 1573
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-08-01
Pay. Date : 2014-07-23
DMF Number : 20894
Submission : 2007-10-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19340
Submission : 2006-04-11
Status : Active
Type : II
Certificate Number : R1-CEP 2007-121 - Rev 01
Issue Date : 2016-06-30
Type : Chemical
Substance Number : 1573
Status : Withdrawn by Holder
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-03-11
Pay. Date : 2019-01-28
DMF Number : 22482
Submission : 2009-02-05
Status : Active
Type : II
Date of Issue : 2019-08-16
Valid Till : 2025-08-15
Written Confirmation Number : WC-0022
Address of the Firm :
NDC Package Code : 50370-0014
Start Marketing Date : 2010-04-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-08-10
Pay. Date : 2014-04-04
DMF Number : 23442
Submission : 2010-01-08
Status : Active
Type : II
NDC Package Code : 50370-0014
Start Marketing Date : 2010-04-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-01-30
Pay. Date : 2016-01-25
DMF Number : 15376
Submission : 2001-04-05
Status : Active
Type : II
Certificate Number : R1-CEP 2001-089 - Rev 01
Issue Date : 2020-05-27
Type : Chemical
Substance Number : 1573
Status : Valid
NDC Package Code : 53069-0560
Start Marketing Date : 2000-04-05
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 : 19372
Submission : 2006-04-19
Status : Active
Type : II
Certificate Number : R1-CEP 2009-139 - Rev 01
Issue Date : 2018-06-18
Type : Chemical
Substance Number : 1573
Status : Valid
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm :
NDC Package Code : 62756-730
Start Marketing Date : 2020-05-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-16
Pay. Date : 2014-05-08
DMF Number : 19330
Submission : 2006-03-31
Status : Active
Type : II
Certificate Number : CEP 2006-193 - Rev 07
Issue Date : 2023-11-14
Type : Chemical
Substance Number : 1573
Status : Valid
Date of Issue : 2022-06-06
Valid Till : 2025-06-10
Written Confirmation Number : WC-0017
Address of the Firm :
NDC Package Code : 59651-151
Start Marketing Date : 2024-01-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-01-10
Pay. Date : 2017-11-14
DMF Number : 32218
Submission : 2017-11-15
Status : Active
Type : II
Certificate Number : CEP 2016-134 - Rev 02
Issue Date : 2024-08-27
Type : Chemical
Substance Number : 1573
Status : Valid
NDC Package Code : 59651-151
Start Marketing Date : 2024-01-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36972
Submission : 2022-07-05
Status : Active
Type : II
Certificate Number : CEP 2022-292 - Rev 00
Issue Date : 2024-09-02
Type : Chemical
Substance Number : 1573
Status : Valid
Date of Issue : 2022-02-02
Valid Till : 2024-06-07
Written Confirmation Number : WC-0317
Address of the Firm :
NDC Package Code : 52562-024
Start Marketing Date : 2022-12-01
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 : 23624
Submission : 2010-03-10
Status : Active
Type : II
Date of Issue : 2019-06-17
Valid Till : 2022-06-16
Written Confirmation Number : WC-0030
Address of the Firm :
NDC Package Code : 62331-048
Start Marketing Date : 2009-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2021-11-15
Registration Number : 20211115-209-J-1150
Manufacturer Name : Divi's Laboratories Limited
Manufacturer Address : Unit-2, Annavaram (Post), Chippada Village, Bheemunipatnam Mandal, Visakhapatnam District –531 162, Andhra Pradesh, India
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-07-02
Pay. Date : 2013-06-21
DMF Number : 20746
Submission : 2007-08-03
Status : Active
Type : II
NDC Package Code : 67835-5010
Start Marketing Date : 2008-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-08-13
Pay. Date : 2013-08-02
DMF Number : 20906
Submission : 2007-10-03
Status : Active
Type : II
NDC Package Code : 67835-5010
Start Marketing Date : 2008-02-13
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 : 21711
Submission : 2008-06-03
Status : Active
Type : II
Registration Number : 223MF10048
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2011-04-06
Latest Date of Registration : --
Date of Issue : 2019-08-05
Valid Till : 2022-08-04
Written Confirmation Number : WC-0118
Address of the Firm :
NDC Package Code : 65015-860
Start Marketing Date : 2015-05-06
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 : 19212
Submission : 2006-03-03
Status : Inactive
Type : II
Certificate Number : R0-CEP 2011-113 - Rev 02
Issue Date : 2017-02-14
Type : Chemical
Substance Number : 1573
Status : Withdrawn by Holder
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24642
Submission : 2011-02-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16903
Submission : 2003-10-20
Status : Inactive
Type : II
NDC Package Code : 53069-0560
Start Marketing Date : 2000-04-05
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 : 17397
Submission : 2004-05-25
Status : Inactive
Type : II
Certificate Number : R0-CEP 2010-167 - Rev 01
Issue Date : 2014-07-28
Type : Chemical
Substance Number : 1573
Status : Withdrawn by Holder
NDC Package Code : 53104-7581
Start Marketing Date : 2016-01-01
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 : 16279
Submission : 2002-12-02
Status : Inactive
Type : II
Certificate Number : R1-CEP 2007-329 - Rev 05
Issue Date : 2019-09-16
Type : Chemical
Substance Number : 1573
Status : Valid
Registration Number : 228MF10195
Registrant's Address : Plot No. 72, H. No.:8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills, Hyderabad, Telangana, India
Initial Date of Registration : 2016-10-11
Latest Date of Registration : --
Date of Issue : 2019-06-26
Valid Till : 2022-07-02
Written Confirmation Number : WC-0071
Address of the Firm :
NDC Package Code : 67835-5010
Start Marketing Date : 2008-02-13
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 : 18287
Submission : 2005-04-19
Status : Inactive
Type : II
Certificate Number : R1-CEP 2004-175 - Rev 04
Issue Date : 2019-09-16
Type : Chemical
Substance Number : 1573
Status : Withdrawn by Holder
NDC Package Code : 67835-5010
Start Marketing Date : 2008-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Sumatriptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sumatriptan, including repackagers and relabelers. The FDA regulates Sumatriptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sumatriptan 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 Sumatriptan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sumatriptan supplier is an individual or a company that provides Sumatriptan active pharmaceutical ingredient (API) or Sumatriptan finished formulations upon request. The Sumatriptan suppliers may include Sumatriptan API manufacturers, exporters, distributors and traders.
click here to find a list of Sumatriptan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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