GEMITA GEMCITABINE INJECTION

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GEMITA GEMCITABINE INJECTION Specification

Origin of Medicine
Imported

Indication
Treatment of ovarian, breast, pancreatic, and non-small cell lung cancer

Pacakaging (Quantity Per Box)
Single vial per box

Dosage Form
Injection

Salt Composition
Gemcitabine Hydrochloride

Drug Type
Prescription only

Ingredients
Gemcitabine Hydrochloride

Physical Form
Liquid Injection

Function

Recommended For
Cancer treatment (including ovarian, breast, non-small cell lung, and pancreatic cancer)

Dosage
As prescribed by the oncologist; dosing varies based on type of cancer and patient condition

Dosage Guidelines
Administered intravenously under the supervision of a qualified physician

Suitable For
Adults

Quantity
1000 mg per vial

Storage Instructions
Store below 25C, protect from light

GEMITA GEMCITABINE INJECTION Trade Information

Packaging Details
PACK OF 1 VIAL

About GEMITA GEMCITABINE INJECTION

Specifications :-

Brand Name :- GEMITA
Content:-Gemcitabine
Strength:- 200 mg
Form:- injection
Packing:- Pack of 1 vial
Manufactured By :- Fresenius Kabi

Note :- GEMITA Is A Prescription Drug And Should Be Used Under Proper Medical Guidance And Advice. Do Not Share The Medicine With Othe...........

Powerful Cancer Therapy

GEMITA is formulated to deliver effective chemotherapy for adults diagnosed with ovarian, breast, pancreatic, or non-small cell lung cancer. Its trusted efficacy and broad indications make it a valuable option for oncologists seeking flexible and powerful cancer management strategies.

Strict Hospital Use and Safety

To ensure maximum safety and efficacy, GEMITA is administered exclusively in hospitals or oncology clinics, supervised by qualified healthcare professionals. Its intravenous route allows for controlled dosing tailored to individual patient needs, minimizing risk and maximizing therapeutic benefits.

Easy Preparation and Storage

Provided as a clear solution in single-vial packaging, GEMITA requires reconstitution with sterile saline before infusion. The injection must be stored below 25C and shielded from light, ensuring its stability and readiness for use throughout its two-year shelf life.

FAQs of GEMITA GEMCITABINE INJECTION:

Q: How should GEMITA Gemcitabine Injection be prepared for administration?

A: GEMITA should be reconstituted using sterile saline, following aseptic techniques, just before intravenous infusion as directed by hospital staff or oncology clinic personnel.

Q: What types of cancer are treated with GEMITA Gemcitabine Injection?

A: GEMITA is recommended for adults in the treatment of ovarian cancer, breast cancer, non-small cell lung cancer, and pancreatic cancer, as prescribed by an oncologist.

Q: When is GEMITA Gemcitabine Injection administered during cancer therapy?

A: Administration timing and dosing of GEMITA are determined by the treating oncologist, depending on cancer type, progression, and patient-specific treatment protocols.

Q: Where must GEMITA Gemcitabine Injection be administered?

A: GEMITA is intended for intravenous administration in hospital environments or specialized oncology clinics, under direct supervision of medical professionals.

Q: What is the process for storing GEMITA Gemcitabine Injection?

A: Store GEMITA below 25C, protected from light, and utilize the vial within its two-year shelf life to maintain product potency and safety.

Q: Is a prescription required to obtain GEMITA Gemcitabine Injection?

A: Yes, GEMITA is a prescription-only medication and must be dispensed and administered solely upon medical guidance from a licensed physician.

Q: What are the main benefits of GEMITA Gemcitabine Injection in cancer treatment?

A: GEMITA offers targeted anti-cancer effects, flexible dosing tailored by oncologists, and proven efficacy across multiple cancer types, contributing to improved treatment outcomes under medical supervision.

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