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List of Oncology Medication For

Diabetes

Indian Pharma Network

M: +9891296838 / 9811747774
E: med@indianpharmanetwork.co.in

alogliptin and metformin Tablets

alogliptin and metformin HC tablets
for oral use Initial U.S. Approval: 2013

KAZANO is a dipeptidyl-peptidase-4 (DPP-4) inhibitor and a biguanide combination product indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Facts about alogliptin and metformin Tablets

Approval Date:  2013
Proprietary Name:  KAZANO (alogliptin and metformin HCl) tablets
Active Ingredient(s):  alogliptin and metformin HCl
FDA-approved use:
Dosage Form:  Tablets: 12.5 mg alogliptin and 500 mg metformin HCl, 12.5 mg alogliptin and 1000 mg metformin HCl.
Medicine Approved By: Food and Drug Administration (FDA)
Manufacturer: Takeda Pharmaceuticals
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

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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 “alogliptin and metformin Tablets” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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alogliptin tablets

alogliptin tablets
for oral use Initial U.S. Approval: 2013

NESINA is a dipeptidyl peptidase-4 (DPP-4) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Facts about alogliptin tablets

Approval Date:  2013
Proprietary Name:  NESINA (alogliptin) tablets
Active Ingredient(s):  alogliptin
FDA-approved use: type 2 diabetes mellitus
Dosage Form:  Tablets: 25 mg, 12.5 mg and 6.25 mg
Medicine Approved By: Food and Drug Administration (FDA)
Manufacturer: Takeda Pharmaceuticals
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

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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 “alogliptin tablets” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

 

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dulaglutide injection

dulaglutide injection
for subcutaneous use Initial U.S. Approval: 2014

Facts about dulaglutide injection

Approval Date: 2014
Proprietary Name: On Request
Active Ingredient(s): dulaglutide
Dosage Forms And Strengths: Injection: 0.75 mg/0.5 mL solution in a single-dose pen
Injection: 1.5 mg/0.5 mL solution in a single-dose pen
Injection: 0.75 mg/0.5 mL solution in a single-dose prefilled syringe
Injection: 1.5 mg/0.5 mL solution in a single-dose prefilled syringe
Company: Eli Lilly
Diseases: Type 2 diabetes, cardiovascular risk reduction
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)

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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 “dulaglutide injection” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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empagliflozin and linagliptin tablets

empagliflozin and linagliptin tablets
for oral use Initial U.S. Approval: 2015

Facts about empagliflozin and linagliptin tablets

Approval Date:  2015
Proprietary Name: GLYXAMBI (empagliflozin and linagliptin) tablets
Active Ingredient(s):  empagliflozin and linagliptin
FDA-approved use:
Dosage Form:  Tablets:  • 10 mg empagliflozin/5 mg linagliptin  • 25 mg empagliflozin/5 mg linagliptin
Medicine Approved By: Food and Drug Administration (FDA)
Manufacturer: Boehringer Ingelheim Pharmaceuticals, Inc
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 “empagliflozin and linagliptin tablets” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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empagliflozin tablets

empagliflozin tablets,
for oral use Initial U.S. Approval: 2014

As specified in the prescribing information, empagliflozin tablets is indicated for the treatment of type 2 diabetes mellitus. JARDIANCE is indicated: • as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus, • to reduce the risk of cardiovascular death in adult patients with type 2 diabetes mellitus and established cardiovascular disease.

Facts about empagliflozin tablets

pproval Date: 2014
Proprietary Name: JARDIANCE (empagliflozin) tablets
Active Ingredient(s): empagliflozin
FDA-approved use: type 2 diabetes mellitus
Dosage Form: Tablets: 10 mg, 25 mg
Medicine Approved By: US FDA
Manufacturer: Boehringer Ingelheim Pharmaceuticals, Inc.
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 “empagliflozin tablets” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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ertugliflozin tablets

ertugliflozin tablets
for oral use Initial U.S. Approval: 2017

STEGLATRO is a sodium glucose co-transporter 2 (SGLT2) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Facts about ertugliflozin tablets

Approval Date:  2017
Proprietary Name:  STEGLATRO (ertugliflozin) tablets
Active Ingredient(s):  ertugliflozin tablets
Dosage Form:  Tablets: 5 mg and 15 mg
Medicine Approved By: Food and Drug Administration (FDA)
Manufacturer: Merck Sharp & Dohme Corp.
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 “ertugliflozin tablets” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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exenatide Injection

exenatide Injection
Initial U.S. Approval: 2005

BYETTA is a glucagon-like peptide-1 (GLP-1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Facts about exenatide Injection 

Approval Date:  2005
Proprietary Name:  BYETTA (exenatide) Injection
Active Ingredient(s):  exenatide
FDA-approved use: 2 diabetes mellitus.
Dosage Form:  BYETTA is supplied as 250 mcg/mL exenatide in:  • 5 mcg per dose, 60 doses, 1.2 mL prefilled pen • 10 mcg per dose, 60 doses, 2.4 mL prefilled pen.
Medicine Approved By: Food and Drug Administration (FDA)
Manufacturer: Amylin Pharmaceuticals, Inc.
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)

Full Support:

IPN, Delhi can help with your prescription of the Registered Medical Practitioner (RMP) to get access. Based on your input information received, a step by step guide on how we can help you legally and safely import a medicine “exenatide Injection” will be provided.

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Lixisenatide Injection

Lixisenatide Prefilled Solution for Injection

Lixisenatide is a glucagon-like peptide-1 (GLP-1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Facts about Lixisenatide Injection

Approval Date:  July 27, 2016
Proprietary Name:  Lyxumia Lixisenatide Prefilled Solution for Injection
Active Ingredient(s):  Lixisenatide Prefilled Solution for Injection
FDA-approved use: adults with type 2 diabetes mellitus
Dosage Form:  solution for injection

  • Lyxumia 10 micrograms solution for injection
  • Lyxumia 20 micrograms solution for injection

Medicine Approved By: Food and Drug Administration (FDA), EMA
Manufacturer: sanofi-aventis

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 “Lixisenatide Injection” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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teplizumab-mzwv injection

teplizumab-mzwv injection,
for intravenous use Initial U.S. Approval: 2022

As specified in the prescribing information, teplizumab-mzwv injection is indicated for the treatment of Stage 3 type 1 diabetes disease.  TZIELD is a CD3-directed antibody indicated to delay the onset of Stage 3 type 1 diabetes (T1D) in adults and pediatric patients aged 8 years and older with Stage 2 T1D

Facts about teplizumab-mzwv injection

Approval Date: 11/17/2022
Proprietary Name: Tzield
Active Ingredient(s): teplizumab-mzwv
FDA-approved use: To delay the onset of Stage 3 type 1 diabetes
Dosage Form: Injection: 2 mg per 2 mL (1 mg/mL) single-dose vial.
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 “teplizumab-mzwv injection” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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tirzepatide injection

tirzepatide Injection,
for subcutaneous use Initial U.S. Approval: 2022

As specified in the prescribing information, tirzepatide Injection is indicated for the treatment of diabetes.  MOUNJARO is a glucose-dependent insulinotropic polypeptide (GIP) receptor and glucagon-like peptide-1 (GLP-1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Facts about tirzepatide injection

Approval Date: 5/13/2022
Proprietary Name: Mounjaro
Active Ingredient(s): tirzepatide
FDA-approved use: To improve blood sugar control in diabetes, in addition to diet and exercise
Dosage Form: Injection: 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, or 15 mg per 0.5 mL in single-dose pen
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 “tirzepatide injection” based on the information you provide.

Indian Pharma Network (IPN) Legitimate consultant and facilitator in the New Delhi, India. IPN has over two decades of industry experience and extensive coverage throughout India, including major cities such as Mumbai, Kolkata, Hyderabad, Chennai, Ahmedabad, Delhi, Bangalore, Srinagar, Jammu, Jaipur, Chandigarh, Ludhiana, Noida, Gurgaon, Lucknow, the North East, Pune, and other regions.

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Contact Info

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New Delhi:110016 India.

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Indian Pharma Network (IPN), New Delhi. India

Indian Pharma Network (IPN) is registered organisation in India, having highly qualified healthcare professionals of pharmaceutical Industry. Specialized in Oncology Products. Helped more than 6,000 patients. Registration Number : 07AAFFI2544E1ZO under GST Act.
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