01 1Bristol Myers Squibb
02 1DMFs Not Supported
03 1GOLDEN SHELL BIOCHEMICAL CO LTD
04 1Hainan Poly Pharm
05 1Wanbury Limited
06 1ZHEJIANG ZHOUHUA ORGANISMS SCIENCE AND TECHNOLOGY DEVELOPMENT
07 2ZHOUSHAN PUTO XINXING PHARMACHEM CO LTD
08 1Zhejiang Cheng Yi Pharmaceutical Co., Ltd
09 1Zhejiang Fengrun Biochemical
01 1D-GLUCOSAMINE HYDROCHLORIDE SOLUTION, 2N SODIUM HYDROXIDE SOLUTION
02 1GLUCOSAMINE HCL
03 5GLUCOSAMINE HYDROCHLORIDE
04 1GLUCOSAMINE HYDROCHLORIDE PELLETS CAPSULES
05 2GLUCOSAMINE HYDROCHLORIDE USP
01 7China
02 1India
03 1U.S.A
04 1Blank
01 5Active
02 5Inactive
01 10Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1391
Submission : 1969-07-16
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35716
Submission : 2021-06-12
Status : Active
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 : 23622
Submission : 2010-03-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23487
Submission : 2010-01-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19143
Submission : 2006-01-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33214
Submission : 2018-12-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39278
Submission : 2023-12-21
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22177
Submission : 2008-08-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30685
Submission : 2016-06-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22180
Submission : 2008-08-22
Status : Inactive
Type : II
A Glucosamine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucosamine Hydrochloride, including repackagers and relabelers. The FDA regulates Glucosamine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucosamine 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 Glucosamine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glucosamine Hydrochloride supplier is an individual or a company that provides Glucosamine Hydrochloride active pharmaceutical ingredient (API) or Glucosamine Hydrochloride finished formulations upon request. The Glucosamine Hydrochloride suppliers may include Glucosamine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Glucosamine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glucosamine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Glucosamine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Glucosamine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Glucosamine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Glucosamine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Glucosamine Hydrochloride USDMF includes data on Glucosamine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Glucosamine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Glucosamine Hydrochloride suppliers with USDMF on PharmaCompass.
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