Synopsis
Synopsis
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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Others
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FDA Orange Book
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Canada
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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US Patents
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1. Zinc Dihexonate
2. D-gluconic Acid Zinc (ii) Salt
3. Gluconic Acid Zinc (ii) Salt
4. Dtxsid001002491
5. Ft-0659318
6. Zinc, Bis(d-gluconato-.kappa.o1,.kappa.o2)-, (t-4)-
7. 82139-35-3
| Molecular Weight | 455.7 g/mol |
|---|---|
| Molecular Formula | C12H22O14Zn |
| Hydrogen Bond Donor Count | 10 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 8 |
| Exact Mass | 454.030097 g/mol |
| Monoisotopic Mass | 454.030097 g/mol |
| Topological Polar Surface Area | 283 Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 165 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 8 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36033
Submission : 2021-06-12
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5723
Submission : 1985-02-27
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24707
Submission : 2010-12-20
Status : Inactive
Type : II

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11903
Submission : 1996-03-29
Status : Inactive
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 : 6002
Submission : 1985-07-30
Status : Inactive
Type : II


Certificate Number : R1-CEP 2012-221 - Rev 00
Issue Date : 2019-05-10
Type : Chemical
Substance Number : 2164
Status : Withdrawn by EDQM F...



FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6002
Submission : 1985-07-30
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5723
Submission : 1985-02-27
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24707
Submission : 2010-12-20
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36033
Submission : 2021-06-12
Status : Active
Type : II

USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11903
Submission : 1996-03-29
Status : Inactive
Type : II

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
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Grade : Oral
Application : Fillers, Diluents & Binders
Pharmacopoeia Ref : Conforms to USP-NF, Ph.Eur., J...
Technical Specs : Density- Tapped density- 440 g/l, Bulk density- 280 g/l; Particle size- D10- 25 ?m, D50- 60 ?m, D90-...
Ingredient(s) : Microcrystalline Cellulose Excipients
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Technical Specs : Density- Tapped density- 440 g/l, Bulk density- 310 g/l; Particle size- D10- 40 ?m, D50- 90 ?m, D90...
Ingredient(s) : Microcrystalline Cellulose Excipients
Dosage Form : Orodispersible Tablet
Grade : Oral
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Pharmacopoeia Ref : Conforms to USP-NF, Ph.Eur., J...
Technical Specs : Not Available
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Excipient Details : It is a dextrose monohydrate pyrogen-free that is a physiological sugar used to provide excipient and API benefits.
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Pharmacopoeia Ref : EP/USP/JP
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose Excipients
Dosage Form : Tablet
Grade : Not Available
Application : Disintegrants & Superdisintegrants
Excipient Details : It is a superdisintegrant that provides an efficient disintegration at low level of use
Dosage Form : Cream / Lotion / Ointment
Grade : Not Available
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Excipient Details : A co-processed product used as a secondary stabilizer and suspension agent in semi-solides formulas.
Pharmacopoeia Ref : EP/USP/JP
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose Excipients
Dosage Form : Cream / Lotion / Ointment
Grade : Not Available
Application : Thickeners and Stabilizers
Excipient Details : A co-processed product used as a secondary stabilizer and suspension agent in semi-solides formulas.
Pharmacopoeia Ref : EP/USP/JP
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose Excipients
Dosage Form : Cream / Lotion / Ointment
Grade : Not Available
Application : Thickeners and Stabilizers
Excipient Details : A co-processed product used as a secondary stabilizer and suspension agent in semi-solides formulas.
Pharmacopoeia Ref : EP/USP/JP
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose Excipients
Dosage Form : Cream / Lotion / Ointment
Grade : Not Available
Application : Thickeners and Stabilizers
Excipient Details : A co-processed product used as a secondary stabilizer and suspension agent in semi-solides formulas.
Pharmacopoeia Ref : EP/USP/JP
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose Excipients
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Dosage Form : Tablet
Grade : Oral
Dosage Form : Tablet
Grade : Oral
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Grade : Oral
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Excipients by Applications
Market Place
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PharmaCompass offers a list of Zinc Gluconate API 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 Zinc Gluconate API manufacturer or Zinc Gluconate API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zinc Gluconate API manufacturer or Zinc Gluconate API supplier.
PharmaCompass also assists you with knowing the Zinc Gluconate API API Price utilized in the formulation of products. Zinc Gluconate API API Price is not always fixed or binding as the Zinc Gluconate API Price is obtained through a variety of data sources. The Zinc Gluconate API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A USP ZINC GLUCONATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of USP ZINC GLUCONATE, including repackagers and relabelers. The FDA regulates USP ZINC GLUCONATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. USP ZINC GLUCONATE 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 USP ZINC GLUCONATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A USP ZINC GLUCONATE supplier is an individual or a company that provides USP ZINC GLUCONATE active pharmaceutical ingredient (API) or USP ZINC GLUCONATE finished formulations upon request. The USP ZINC GLUCONATE suppliers may include USP ZINC GLUCONATE API manufacturers, exporters, distributors and traders.
click here to find a list of USP ZINC GLUCONATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A USP ZINC GLUCONATE DMF (Drug Master File) is a document detailing the whole manufacturing process of USP ZINC GLUCONATE active pharmaceutical ingredient (API) in detail. Different forms of USP ZINC GLUCONATE DMFs exist exist since differing nations have different regulations, such as USP ZINC GLUCONATE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A USP ZINC GLUCONATE DMF submitted to regulatory agencies in the US is known as a USDMF. USP ZINC GLUCONATE USDMF includes data on USP ZINC GLUCONATE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The USP ZINC GLUCONATE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of USP ZINC GLUCONATE suppliers with USDMF on PharmaCompass.
A USP ZINC GLUCONATE CEP of the European Pharmacopoeia monograph is often referred to as a USP ZINC GLUCONATE Certificate of Suitability (COS). The purpose of a USP ZINC GLUCONATE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of USP ZINC GLUCONATE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of USP ZINC GLUCONATE to their clients by showing that a USP ZINC GLUCONATE CEP has been issued for it. The manufacturer submits a USP ZINC GLUCONATE CEP (COS) as part of the market authorization procedure, and it takes on the role of a USP ZINC GLUCONATE CEP holder for the record. Additionally, the data presented in the USP ZINC GLUCONATE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the USP ZINC GLUCONATE DMF.
A USP ZINC GLUCONATE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. USP ZINC GLUCONATE CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of USP ZINC GLUCONATE suppliers with CEP (COS) on PharmaCompass.
USP ZINC GLUCONATE Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of USP ZINC GLUCONATE GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right USP ZINC GLUCONATE GMP manufacturer or USP ZINC GLUCONATE GMP API supplier for your needs.
A USP ZINC GLUCONATE CoA (Certificate of Analysis) is a formal document that attests to USP ZINC GLUCONATE's compliance with USP ZINC GLUCONATE specifications and serves as a tool for batch-level quality control.
USP ZINC GLUCONATE CoA mostly includes findings from lab analyses of a specific batch. For each USP ZINC GLUCONATE CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
USP ZINC GLUCONATE may be tested according to a variety of international standards, such as European Pharmacopoeia (USP ZINC GLUCONATE EP), USP ZINC GLUCONATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (USP ZINC GLUCONATE USP).