01 1ACIC Europe API & Pharmaceuticals
02 1Cyclo Industries
03 5Forest Laboratories
04 1Laboratorio Chimico Internazionale Spa
05 1Trifarma
06 5Blank
01 1PROCEDURES FOR THE MANUF OF THIORIDAZINE HCL
02 1THIORIDAZINE HCL
03 1THIORIDAZINE HCL 200 MG C.R. TABS (IN SYNCHRON VEHICLE)
04 1THIORIDAZINE HCL 400MG S.R.TABS (IN SYNCHRON VEHICLE)
05 1THIORIDAZINE HCL USP
06 1THIORIDAZINE HCL USP XXI
07 1THIORIDAZINE HCL. 50MG.C.R.TABLETS
08 1THIORIDAZINE HCL100MG CR(LD IN SYCHRON VEHICLE)MNFG INWOOD,NY
09 1THIORIDAZINE HCl C.R. TABLETS (IN SYNCHRON VEHICLE)
10 3THIORIDAZINE HYDROCHLORIDE
11 1THIORIDAZINE HYDROCHLORIDE USP
12 1THIORIDAZINE hcl
01 1Cyprus
02 2Italy
03 6U.S.A
04 5Blank
01 1Active
02 13Inactive
01 14Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4346
Submission : 1981-10-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4460
Submission : 1982-03-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5702
Submission : 1985-02-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5638
Submission : 1984-11-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4632
Submission : 1982-07-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4624
Submission : 1982-07-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5422
Submission : 1984-06-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4120
Submission : 1981-02-27
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2528
Submission : 1975-09-17
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 : 5613
Submission : 1984-11-29
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
86
PharmaCompass offers a list of Thioridazine 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 Thioridazine Hydrochloride manufacturer or Thioridazine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Thioridazine Hydrochloride manufacturer or Thioridazine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Thioridazine Hydrochloride API Price utilized in the formulation of products. Thioridazine Hydrochloride API Price is not always fixed or binding as the Thioridazine Hydrochloride Price is obtained through a variety of data sources. The Thioridazine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Melleril (tablet) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Melleril (tablet), including repackagers and relabelers. The FDA regulates Melleril (tablet) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Melleril (tablet) 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 Melleril (tablet) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Melleril (tablet) supplier is an individual or a company that provides Melleril (tablet) active pharmaceutical ingredient (API) or Melleril (tablet) finished formulations upon request. The Melleril (tablet) suppliers may include Melleril (tablet) API manufacturers, exporters, distributors and traders.
click here to find a list of Melleril (tablet) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Melleril (tablet) DMF (Drug Master File) is a document detailing the whole manufacturing process of Melleril (tablet) active pharmaceutical ingredient (API) in detail. Different forms of Melleril (tablet) DMFs exist exist since differing nations have different regulations, such as Melleril (tablet) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Melleril (tablet) DMF submitted to regulatory agencies in the US is known as a USDMF. Melleril (tablet) USDMF includes data on Melleril (tablet)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Melleril (tablet) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Melleril (tablet) suppliers with USDMF on PharmaCompass.
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