01 1Merck Serono
02 1Sandoz B2B
03 1Siegfried AG
04 1Vasudha Pharma Chem
05 2Blank
01 5DIBENZOSUBERONE
02 1DIBENZOSUBERONE BULK FORM
01 1Germany
02 1India
03 2Switzerland
04 2Blank
01 1Active
02 5Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3460
Submission : 1979-03-07
Status : Inactive
Type : II
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
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32893
Submission : 2018-08-31
Status : Active
Type : II
USDMF
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
USDMF
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
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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.
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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.
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A AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] DMF (Drug Master File) is a document detailing the whole manufacturing process of AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] active pharmaceutical ingredient (API) in detail. Different forms of AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] DMFs exist exist since differing nations have different regulations, such as AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] DMF submitted to regulatory agencies in the US is known as a USDMF. AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] USDMF includes data on AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY] USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 4 companies offering AMITRIPTYLINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
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