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
A Cyproheptadine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyproheptadine Hydrochloride, including repackagers and relabelers. The FDA regulates Cyproheptadine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyproheptadine Hydrochloride 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 Cyproheptadine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyproheptadine Hydrochloride supplier is an individual or a company that provides Cyproheptadine Hydrochloride active pharmaceutical ingredient (API) or Cyproheptadine Hydrochloride finished formulations upon request. The Cyproheptadine Hydrochloride suppliers may include Cyproheptadine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cyproheptadine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cyproheptadine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Cyproheptadine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Cyproheptadine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Cyproheptadine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cyproheptadine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Cyproheptadine Hydrochloride USDMF includes data on Cyproheptadine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cyproheptadine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cyproheptadine Hydrochloride suppliers with USDMF on PharmaCompass.
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