Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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01 1Supriya Lifescience
02 1Virupaksha Organics
03 1Aragen Life Sciences
04 1Arevipharma
05 1Aurobindo Pharma Limited
06 2CSPC Pharmaceutical Group
07 1Catalytica
08 1Dai-ichi Kogyo Seiyaku
09 1Dipharma
10 1Dishman Carbogen Amcis
11 1Emnar Pharma
12 2Grunenthal
13 1Helsinn Advanced Synthesis
14 2Ipca Laboratories
15 1Jubilant Generics
16 1KAMUD DRUGS PVT LTD
17 1Macleods Pharmaceuticals Limited
18 1Piramal Pharma Solutions
19 1ROUGIER PHARMA DIVISION OF RATIOPHARM INC
20 2Raks Pharma
21 1Recordati
22 1SEQUEL PHARMACHEM PRIVATE LTD. IN 400 706 Nerul
23 1SHIJIAZHUANG NO.4 PHARMACEUTICAL CO., LT
24 2Sun Pharmaceutical Industries Limited
25 1TONIRA PHARMA LTD
26 1Unichem Laboratories Limited
27 1Wanbury Limited
28 1Zentiva
29 2Zydus Lifesciences
30 1Blank
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01 1CONTRAMID
02 1TRAMADOL HCL
03 1TRAMADOL HYDROCHLORID EP
04 16TRAMADOL HYDROCHLORIDE
05 1TRAMADOL HYDROCHLORIDE (YT3 PROCESS)
06 1TRAMADOL HYDROCHLORIDE BP
07 2TRAMADOL HYDROCHLORIDE EP
08 9TRAMADOL HYDROCHLORIDE USP
09 1TRAMADOL HYDROCHLORIDE USP (BULK)
10 1TRAMADOL HYDROCHLORIDE USP (NON STERILE DRUG SUBSTANCE)
11 1TRAMADOL HYDROCHLORIDE USP API (PROCESS-2)
12 1Tramadol Hydrochloride USP (Process-II)
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01 1Canada
02 3China
03 1Czech Republic
04 3Germany
05 22India
06 2Italy
07 1Japan
08 1Switzerland
09 1U.S.A
10 1Blank
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01 18Active
02 18Inactive
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01 12Complete
02 24Blank
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39533
Submission : 2024-02-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-08-01
Pay. Date : 2018-02-20
DMF Number : 30504
Submission : 2016-04-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-11
Pay. Date : 2013-06-14
DMF Number : 20632
Submission : 2007-06-26
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-07-13
Pay. Date : 2018-06-11
DMF Number : 21805
Submission : 2008-07-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15545
Submission : 2001-07-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17166
Submission : 2004-02-18
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-09-21
Pay. Date : 2013-09-12
DMF Number : 18803
Submission : 2005-09-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16002
Submission : 2002-06-06
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-17
Pay. Date : 2013-03-06
DMF Number : 17970
Submission : 2005-01-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17037
Submission : 2004-02-17
Status : Active
Type : II
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PharmaCompass offers a list of Tramadol Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tramadol Hydrochloride manufacturer or Tramadol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tramadol Hydrochloride manufacturer or Tramadol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Tramadol Hydrochloride API Price utilized in the formulation of products. Tramadol Hydrochloride API Price is not always fixed or binding as the Tramadol Hydrochloride Price is obtained through a variety of data sources. The Tramadol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tramol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tramol, including repackagers and relabelers. The FDA regulates Tramol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tramol 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 Tramol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tramol supplier is an individual or a company that provides Tramol active pharmaceutical ingredient (API) or Tramol finished formulations upon request. The Tramol suppliers may include Tramol API manufacturers, exporters, distributors and traders.
click here to find a list of Tramol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tramol DMF (Drug Master File) is a document detailing the whole manufacturing process of Tramol active pharmaceutical ingredient (API) in detail. Different forms of Tramol DMFs exist exist since differing nations have different regulations, such as Tramol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tramol DMF submitted to regulatory agencies in the US is known as a USDMF. Tramol USDMF includes data on Tramol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tramol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tramol suppliers with USDMF on PharmaCompass.
We have 29 companies offering Tramol
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