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Glutathione for Injection 1200mg/ 15ml Vial or 20ml Vial Whitening Antitumor Adjuvant Gsh
| Price | Negotiable |
|---|---|
| Min Order | 10000 vial |
| Availability | In Stock |
| Shipping From | Hubei, China |
| Popularity | 392 people viewed |
Model NO.:
1200mg/15ml vial 1200mg/20ml vial
Application:
Injection
Usage Mode:
IV
Suitable for:
Adult
State:
Solid
Shape:
Powder
Type:
Biological Products
Pharmaceutical Technology:
Chemical Synthesis
Chemical Formula:
C10h17n3o6s
Molecular Weight:
307.32300
Melting Point:
182-192 Degree
Boiling Point:
410.1 Degrees
Character:
White Lyophilized Powder
Trademark:
Without
Transport Package:
Carton
Specification:
1200mg/15ml vial 1200mg/20ml vial
Origin:
China
HS Code:
3004909099
Product Description
Indication
It is used for the prevention and treatment of tissue and cell damage caused by drugs (such as chemotherapy drugs, antituberculosis drugs, psychiatric drugs, paracetamol, etc.), radiotherapy, alcohol, organic phosphorus, etc.
It has a protective effect on liver damage caused by various reasons.
Usage and dosage
This product can be intramuscularly injected, or slowly intravenously injected, or added to the infusion intravenous drip, or according to the doctor's order 1-2 per day.
Certificate of Analysis
| Product Name | Glutathione for Injection | ||||
| Batch No. | Sample | Specification | 1200mg/15ml | ||
| Number | Without | Quantity | 300vials | ||
| Test items | Quality Standard | Test Result | |||
| Characteristics | White lyophilized powder | Complies | |||
| Identification | |||||
| Identification by HPLC | The retention time of the main peak of the test solution should be the same as that of the reduced glutathione control solution | Complies | |||
| Sodium salt identification | Should be positive | Positive | |||
| Inspect | |||||
| PH | PH should be 4.8~7.0 | 5.2 | |||
| Loss on drying | Should not be exceed 6.0% | 5.2% | |||
| Dissolution time limit | Should be completely dissolved within one minute. | Complies | |||
| Related substances | The sum of various impurities shall not exceed 5.0% . | 2.1% | |||
| Bacterial endotoxin | Should be less than 0.4EU for each 1mg endotoxin | Complies | |||
| Content Uniformity | Should be meet requirement | Complies | |||
| Visible Particles | Should be meet requirement | Complies | |||
| Insoluble particles | Should be meet requirement | Complies | |||
| Sterile | Should be meet requirement | Complies | |||
| Assay | It should be contains glutathione(C10H17N3O6S) 95.0%~104.0% of labeled amount. | 96.3% | |||
| Conclusions:The product complies with the requirement of CP standard. | |||||
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