List of Oncology Medication For

Lung Cancer

The most commonly diagnosed type of lung cancer is carcinoma. There are many types of carcinoma-derived lung cancers, but the significant types are classified as small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). SCLC and NSCLC are the second cancer leaders. In comparison to NSCLC, SCLC can proliferate and form solid tumor masses more rapidly. In contrast with this highly proliferative potential, SCLC is known to be less aggressive than non-small lung malignancies.

If Lung Cancer Medicines are not yet approved or available in your area, you may give a request, to get access price in India under a specific brand name through IPN. For assistance and guidance, you can contact us by providing complete details. Our pharmaceutical expert will help you find a suitable and practical solution to your query. To receive comprehensive support, please call us at +91 9891 296 838 (Mr. Tarun) / +91 9811 747 774 (Mr. Neeraj).

LAZCLUZE (lazertinib) tablets

Lung Cancer

Brand Name: LAZCLUZE Generic Name: lazertinib LAZCLUZE (lazertinib) is used to treat non-small cell lung cancer (NSCLC) .

LAZCLUZE is prescription medicines. On August 19, 2024, the Food and Drug Administration approved lazertinib (Lazcluze, Janssen Biotech, Inc.) in combination with amivantamab-vmjw (Rybrevant, Janssen Biotech, Inc.) for the first-line treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC).

Brand Name:	LAZCLUZE
Generic Name:	lazertinib
Strength:	Tablets: 80 mg and 240 mg
Manufacturer:	Janssen Biotech
Approved By:	EMA, USFDA

Source Details: Patient Information

IPN, New Delhi can facilitate patient to import of “LAZCLUZE (lazertinib)” in small quantities for personal use. For this applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP). If you have any question, please email IPN healthcare Support Team for LAZCLUZE (lazertinib) price list or cost in India. on Mr. Tarun:- +91 9891 296 838 / Mr. Neeraj:- +91 9811 747 774.

Lorviqua Tablets

Lung Cancer

Lorviqua 25 mg film-coated tablets

Lorviqua (lorlatinib) is a medicine indicated for the treatment of previously treated patients with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC). The medicine is marketed in the USA under the brand name Lorbrena, and in the EU under the brand name Lorviqua. We can help you obtain Lorviqua (lorlatinib) on our website.

Facts about Lorviqua tablets

Disease Indications-Lung Cancer
Manufacturer-Pfizer Limited
Usage-Oral
Medicine Approved By-European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada, Therapeutic Goods Administration (TGA)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “Lorviqua tablets” based on the information you provide.

Indian Pharma Network (IPN) serves as a legitimate consultant and facilitator situated in New Delhi, India. With over two decades of industry experience, IPN offers extensive coverage across India, including prominent cities such as Mumbai, Delhi, Kolkata, Bhubaneswar, Bangalore, Hyderabad, Chennai, Ahmedbad, Pune, Surat, Visakhapatnam, Jaipur, Lucknow, Nagpur, Indore, Patna, Agartala, Guwahati, Imphal, Kohima, Namchi, Noida, Ghaziabad, Ludhiana, Agra, Varanasi, Srinagar, Amritsar, Jodhpur, Chandigarh, Gurgaon, Gorakhpur, Dehradun, Jammu, Hyderabad, Thiruvananthapuram, Kochi, Coimbatore, Puducherry, Mysuru, Salem, Vellore, Tiruppur, Guntur, Goa, Kolhapur, Mumbai, Nashik, and various other regions in India.

Lurbinectedin-Solution

Lung Cancer

Zepzelca 4 Mg Intravenous Solution
Alkylating Agents

Zepzelca (lurbinectedin) is a medication used for the treatment of adult patients with metastatic small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy.

Facts about Lurbinectedin-solution

Disease Indications-Lung Cancer
Manufacturer-Jazz Pharmaceuticals
Usage-Intravenous
Medicine Approved By-Food and Drug Administration (FDA)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “Lurbinectedin-solution” based on the information you provide.

Mektovi (Binimetinib) Tablets

Lung Cancer, Skin, Solid Tumors

Brand Name: Mektovi. Generic Name: (Binimetinib). It is used to treat melanoma and non-small cell lung cancer (NSCLC).

Mektovi is used in combination with another medicine, encorafenib , to treat:

melanoma (a skin cancer) that has spread or cannot be removed by surgery;
a type of lung cancer called non-small cell lung cancer (NSCLC). It is used when the cancer is advanced and has the BRAF V600E version of the mutation.

Brand Name:	Mektovi
Generic Name:	Binimetinib
Strength:	• Tablets: 15 mg.
Manufacturer:	Pfizer Inc.
Approved By:	EMA, USFDA

Source Details: Patient Information

IPN, New Delhi can facilitate patient to import of “Mektovi (Binimetinib) Tablets” in small quantities for personal use. For this applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP). If you have any question, please email IPN healthcare Support Team for pharma product cost in India. on Mr. Tarun:- +91 9891 296 838 / Mr. Neeraj:- +91 9811 747 774.

naxitamab-gqgk injection

Lung Cancer

naxitamab-gqgk injection
for intravenous use Initial U.S. Approval: 2020

Danyelza (naxitamab-gqgk) is a medication used to treat children aged 1 year or older and adults with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow.

Facts about naxitamab-gqgk injection

DISEASE INDICATIONS-Neuroblastoma
MANUFACTURER-Y-mAbs Therapeutics
USAGE-Intravenous
Dosage Forms and Strengths: Injection: 40 mg/10 mL (4 mg/mL) in a single-dose vial.
MEDICINE APPROVED BY-Food and Drug Administration (FDA)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “naxitamab-gqgk injection” based on the information you provide.

necitumumab injection

Lung Cancer

necitumumab injection
for intravenous use Initial U.S. Approval: 2015

Portrazza (necitumumab) is a medication used for the treatment of metastatic squamous non-small cell lung cancer. This medicine has been approved in The US, Canda and Europe. We can get you the US FDA approved stock.

Facts about necitumumab injection

DISEASE INDICATIONS-Lung Cancer
MANUFACTURER-Eli Lilly Nederland B.V.
USAGE-Intravenous
MEDICINE APPROVED BY-European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “necitumumab injection” based on the information you provide.

Nintedanib Capsules

Lung Cancer

nintedanib capsules
for oral use Initial U.S. Approval: 2014

OFEV is a kinase inhibitor indicated for the treatment of idiopathic pulmonary fibrosis (IPF).

Facts about nintedanib capsules

Approval Date: 2014
Proprietary Name: On Request
Active Ingredient(s): nintedanib capsules
Dosage Forms And Strengths: Capsules: 150 mg and 100 mg
Company: Boehringer Ingelheim Pharmaceuticals, Inc.
Current indications: idiopathic pulmonary fibrosis (IPF).
Medicine Approved By: – European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada, Therapeutic Goods Administration (TGA), Medsafe (NZ)
Summary of FDA approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “nintedanib capsules” based on the information you provide.

Opdivo Qvantig (nivolumab and hyaluronidase-nvhy) Injection

Kidney, Chronic Disease, Colon, Esophageal, Gastrointestinal, Head And Neck, Lung Cancer, Solid Tumors, Urothelial Carcinoma

Brand Name: Opdivo Qvantig. Generic Name: (nivolumab and hyaluronidase-nvhy). It is used to treat Renal Cell Carcinoma (RCC), Melanoma, Non-Small Cell Lung Cancer (NSCLC), Squamous Cell Carcinoma of the Head and Neck (SCCHN), Urothelial Carcinoma (UC), Colorectal Cancer, Hepatocellular Carcinoma (HCC), Esophageal Cancer, Gastric Cancer, Gastroesophageal Junction Cancer, and Esophageal Adenocarcinoma..

OPDIVO QVANTIG is a combination of nivolumab, a programmed death receptor-1 (PD-1)-blocking antibody, and hyaluronidase, an endoglycosidase, indicated for the treatment of Renal Cell Carcinoma (RCC), Melanoma, Non-Small Cell Lung Cancer (NSCLC), Squamous Cell Carcinoma of the Head and Neck (SCCHN), Urothelial Carcinoma (UC), Colorectal Cancer, Hepatocellular Carcinoma (HCC), Esophageal Cancer, Gastric Cancer, Gastroesophageal Junction Cancer, and Esophageal Adenocarcinoma.

Brand Name:	Opdivo Qvantig
Generic Name:	nivolumab and hyaluronidase-nvhy
Strength:	• Injection: 600 mg nivolumab and 10,000 units hyaluronidase per 5 mL (120 mg/2,000 units per mL) in a single-dose vial.
Manufacturer:	Bristol-Myers Squibb
Approved By:	EMA, USFDA

Source Details: Patient Information

IPN, New Delhi can facilitate patient to import of “Opdivo Qvantig (nivolumab and hyaluronidase-nvhy) Injection” in small quantities for personal use. For this applicant is required to make an application in Form 12A, along with the prescription of the Registered Medical Practitioner (RMP). If you have any question, please email IPN healthcare Support Team for pharma product cost in India. on Mr. Tarun:- +91 9891 296 838 / Mr. Neeraj:- +91 9811 747 774.

ORKAMBI (lumacaftor/ivacaftor) tablets

Lung Cancer

ORKAMBI (lumacaftor/ivacaftor) tablets

ORKAMBI is a combination of lumacaftor and ivacaftor, a cystic fibrosis transmembrane conductance regulator (CFTR) potentiator, indicated for the treatment of cystic fibrosis (CF) in patients age 2 years and older who are homozygous for the F508del mutation in the CFTR gene. If the patient’s genotype is unknown, an FDA-cleared CF mutation test should be used to detect the presence of the F508del mutation on both alleles of the CFTR gene.

Brand Name:	ORKAMBI
Generic Name:	lumacaftor/ivacaftor
Strength:	• Tablets: lumacaftor 100 mg and ivacaftor 125 mg; lumacaftor 200 mg and ivacaftor 125 mg. • Oral granules: Unit-dose packets of lumacaftor 75 mg and ivacaftor 94 mg; lumacaftor 100 mg and ivacaftor 125 mg; lumacaftor 150 mg and ivacaftor 188 mg.
Manufacturer:	Vertex Pharmaceuticals
Approved By:	EMA, USFDA

Source Details: Patient Information

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import ORKAMBI (lumacaftor/ivacaftor) tablets” based on the information you provide.

osimertinib tablet

Lung Cancer

osimertinib tablet
for oral use Initial U.S. Approval: 2015

Tagrisso (osimertinib) is a medicine for the treatment of patients with metastatic non-small cell lung cancer (NSCLC) with a T790M mutation in the epidermal growth factor receptor (EGFR) gene.

Facts about osimertinib tablet

DISEASE INDICATIONS- non-small cell lung cancer
MANUFACTURER-AstraZeneca AB
USAGE-Oral Tablets: 80 mg and 40 mg
MEDICINE APPROVED BY-European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada, Therapeutic Goods Administration (TGA), Medsafe (NZ)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Access the best support services globally

If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “osimertinib tablet” based on the information you provide.

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Shipped Anti-Cancer Medicines.

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Lung Cancer

Brand Name: LAZCLUZE Generic Name: lazertinib LAZCLUZE (lazertinib) is used to treat non-small cell lung cancer (NSCLC) .

Lorviqua 25 mg film-coated tablets

Facts about Lorviqua tablets

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Zepzelca 4 Mg Intravenous Solution Alkylating Agents

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Brand Name: Mektovi. Generic Name: (Binimetinib). It is used to treat melanoma and non-small cell lung cancer (NSCLC).

naxitamab-gqgk injection for intravenous use Initial U.S. Approval: 2020

Facts about naxitamab-gqgk injection

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necitumumab injection for intravenous use Initial U.S. Approval: 2015

Facts about necitumumab injection

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nintedanib capsules for oral use Initial U.S. Approval: 2014

Facts about nintedanib capsules

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ORKAMBI (lumacaftor/ivacaftor) tablets

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osimertinib tablet for oral use Initial U.S. Approval: 2015

Facts about osimertinib tablet

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Privacy Policy

Health Information

Shipped Anti-Cancer Medicines.

Indian Pharma Network (IPN), New Delhi. India

Zepzelca 4 Mg Intravenous Solution
Alkylating Agents

naxitamab-gqgk injection
for intravenous use Initial U.S. Approval: 2020

necitumumab injection
for intravenous use Initial U.S. Approval: 2015

nintedanib capsules
for oral use Initial U.S. Approval: 2014

osimertinib tablet
for oral use Initial U.S. Approval: 2015