01 1Changzhou Siyao Pharmaceuticals
02 1Dipharma
03 1Siegfried AG
04 1Sifavitor srl
05 1Vasudha Pharma Chem
01 1CYPROHEPTADINE HCL USP
02 2CYPROHEPTADINE HCL, USP
03 2CYPROHEPTADINE HYDROCHLORIDE
01 1China
02 1India
03 2Italy
04 1Switzerland
01 3Active
02 2Inactive
01 3Complete
02 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17364
Submission : 2004-02-20
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-04-23
Pay. Date : 2013-04-09
DMF Number : 3524
Submission : 1979-02-08
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3382
Submission : 1978-11-02
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-05-15
Pay. Date : 2012-11-26
DMF Number : 3293
Submission : 1978-09-13
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-06-28
Pay. Date : 2012-12-19
DMF Number : 25456
Submission : 2011-10-10
Status : Active
Type : II
87
PharmaCompass offers a list of Cyproheptadine 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 Cyproheptadine Hydrochloride manufacturer or Cyproheptadine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyproheptadine Hydrochloride manufacturer or Cyproheptadine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cyproheptadine Hydrochloride API Price utilized in the formulation of products. Cyproheptadine Hydrochloride API Price is not always fixed or binding as the Cyproheptadine Hydrochloride Price is obtained through a variety of data sources. The Cyproheptadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Viternum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Viternum, including repackagers and relabelers. The FDA regulates Viternum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Viternum 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 Viternum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Viternum supplier is an individual or a company that provides Viternum active pharmaceutical ingredient (API) or Viternum finished formulations upon request. The Viternum suppliers may include Viternum API manufacturers, exporters, distributors and traders.
click here to find a list of Viternum suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Viternum DMF (Drug Master File) is a document detailing the whole manufacturing process of Viternum active pharmaceutical ingredient (API) in detail. Different forms of Viternum DMFs exist exist since differing nations have different regulations, such as Viternum USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Viternum DMF submitted to regulatory agencies in the US is known as a USDMF. Viternum USDMF includes data on Viternum's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Viternum USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Viternum suppliers with USDMF on PharmaCompass.
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