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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32893
Submission : 2018-08-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3460
Submission : 1979-03-07
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3091
Submission : 1977-12-12
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6683
Submission : 1986-11-21
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4513
Submission : 1982-03-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3075
Submission : 1977-11-21
Status : Inactive
Type : II
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PharmaCompass offers a list of Dibenzsuberone 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 Dibenzsuberone manufacturer or Dibenzsuberone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dibenzsuberone manufacturer or Dibenzsuberone supplier.
PharmaCompass also assists you with knowing the Dibenzsuberone API Price utilized in the formulation of products. Dibenzsuberone API Price is not always fixed or binding as the Dibenzsuberone Price is obtained through a variety of data sources. The Dibenzsuberone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY], including repackagers and relabelers. The FDA regulates AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] supplier is an individual or a company that provides AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] active pharmaceutical ingredient (API) or AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] finished formulations upon request. The AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] suppliers may include AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] API manufacturers, exporters, distributors and traders.
click here to find a list of AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 4 companies offering AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
Get in contact with the supplier of your choice: