Pantoprazole sodium for injection

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Baiyu Pharmaceutical Co., Ltd.

Business Type:Manufacturer

Country/Region:China

Ddu Verified

HOT Rank

8/10

Product Information

  • Indication:Duodenal ulcer, gastrohelcosis, moderate and severe reflux esophagitis, acute upper gastrointestinal bleeding caused by duodenal ulcer, gastrohelcosis, acute gastric mucosal lesion, complex gastrohelc
  • Specification:40mg; 80mg
  • Dosage Form:Injection
  • Active Ingredients:Pantoprazole Sodium
  • Route of Administration:Intravenous Drip
  • Shelf Life:2 years
  • Storage:Sealed
  • Package:Unopened glass vials, 10 vials/box, 100 boxes/carton (Can be customized)
  • Place of Origin:China
  • Qualification:EU GMP

Description

It is supplied as a freeze-dried powder in a clear glass vial fitted with a rubber stopper, for intravenous administration only.

 

Key words: digestive  gastrointestinal  pantoprazole


Active ingredient: Pantoprazole Sodium
Description: White or off-white porous mass or (and) powder.

Dosage Form: lyophilized powder for injection
Indications: Duodenal ulcer, gastrohelcosis, moderate and severe reflux esophagitis, acute upper gastrointestinal bleeding caused by duodenal ulcer, gastrohelcosis, acute gastric mucosal lesion, complex gastrohelcosis, etc.
Strength: 40mg; 80mg (on the basis of C16H14F2N3NaO4S)

Packaging: Unopened glass vials, 10 vials/box, 100 boxes/carton (Can be customized).
Dosage and administration
Pantoprazole sodium for injection is only a short-term (usually no more than 7 to 10 days) treatment for patients not suitable for oral medication. Once the patient can take the drug orally, do not continue to use it.
(1) Duodenal ulcer, gastrohelcosis, moderate and severe reflux esophagitis, acute upper gastrointestinal bleeding caused by duodenal ulcer, gastrohelcosis, acute gastric mucosal lesion, and complex gastrohelcosis: once 40mg to 80mg, 1 to 2 times a day. Prior to use, add 10ml of 0.9% sodium chloride injection into the vial to dissolve the freeze-dried content completely, then be added into 100 to 250ml of 0.9% sodium chloride injection for dilution, next followed by the intravenous infusion. The whole intravenous infusion period should be controlled within 15 to 60 minutes.
(2) Duodenal ulcer, gastrohelcosis, moderate and severe reflux esophagitis: once 40mg, once a day. Prior to use, add 10ml of 0.9% sodium chloride injection into the vial to dissolve the content completely, the dissolved solution can be used directly by intravenous infusion with a whole infusion period more than 2 minutes, or be added into a 100ml of 0.9% sodium chloride injection for dilution, then followed by the intravenous infusion. The whole infusion period should be controlled more than 15 minutes.
After the product is dissolved and diluted, it must be used within 4 hours. Do not use other solvents or other drugs to dissolve and dilute.
Contraindication
People who are allergic to this product or benzimidazole are prohibited from using this drug.

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