Pharmaceutical Exports from India

WHO-GMP certified manufacturer in Panchkula, India. Written rate per pack against your product list.

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39export approvals to USP and BP monographs
In-houserotogravure printing for blister foil and cartons
750+product approvals, all dosage forms
WHO-GMPsite certificate, FDA Haryana, October 2024
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Markets we can register and supply in, shown in blue. India in navy.

Vibcare Healthcare makes tablets, capsules and oral liquids for export from its own WHO-GMP certified plant at Dabkori, Panchkula. 39 products are approved for export to USP and BP monographs. We can register and supply in 38 markets across Africa, Asia and Latin America. Registration documentation, stability data and export packing are handled at the site.

Markets we can supply

38 countries, grouped by region and regulatory bloc

Africa

West Africa: Nigeria, Ghana, Côte d’Ivoire, Benin, Mali, Burkina Faso, Senegal, Sierra Leone
East Africa: Kenya, Tanzania, Uganda, Ethiopia, Sudan, Madagascar, Mauritius
Southern Africa: Zimbabwe, Zambia, Mozambique, Angola
Central Africa: Cameroon, DR Congo

Asia

South Asia: Nepal, Bhutan, Afghanistan, Sri Lanka
Central Asia: Uzbekistan, Tajikistan, Kazakhstan
ASEAN: Myanmar, Philippines, Vietnam, Thailand
West Asia: Yemen, Iraq

Latin America

Central America: El Salvador, Guatemala, Dominican Republic
South America: Venezuela

Registration in further Latin American markets is taken up against a confirmed importer and dossier requirement.

Export approvals on the licence

39 products written to USP and BP monographs: 34 tablets, 4 capsules, 1 oral suspension

Cardiovascular
Amlodipine tablets USP 5 mg and 10 mg, atorvastatin tablets BP 10 mg and 20 mg, bisoprolol fumarate tablets USP 2.5 mg and 5 mg, carvedilol tablets USP 3.125 mg and 6.25 mg, losartan tablets USP 50 mg, propranolol tablets USP/BP 10 mg and 40 mg, rosuvastatin tablets BP 10 mg, telmisartan tablets BP 20 mg
Anti-infective
Azithromycin tablets USP 250 mg and 500 mg, azithromycin oral suspension USP 200 mg, ciprofloxacin tablets BP 500 mg, levofloxacin tablets USP 500 mg, linezolid tablets USP 600 mg, moxifloxacin tablets BP 400 mg, norfloxacin tablets BP 400 mg, rifaximin tablets BP 550 mg
Gastro-intestinal
Esomeprazole gastro-resistant tablets BP 20 mg and 40 mg, omeprazole gastro-resistant capsules BP 20 mg, pantoprazole gastro-resistant tablets USP 40 mg, ranitidine tablets BP 150 mg, ursodeoxycholic acid tablets BP 300 mg
CNS, pain and steroid
Levetiracetam tablets USP 500 mg, pregabalin capsules BP 75 mg, duloxetine delayed-release capsules USP 20 mg, paracetamol tablets BP 500 mg, ibuprofen tablets BP 400 mg, methylprednisolone tablets USP 4 mg
Anti-allergic
Cetirizine tablets BP 10 mg, levocetirizine tablets USP 5 mg, desloratadine tablets USP 5 mg
Metabolic and urology
Metformin prolonged-release tablets BP 1000 mg, tamsulosin modified-release capsules BP 400 mcg

A product not on this list can be added: the export approval is applied for from FDA Haryana against your market and monograph, and stability is set down in our own chambers for the climatic zone of the market.

Product list PDF

Send your product list for a written proposal

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Documentation for registration

What travels with a dossier and with every consignment

Site documents

WHO-GMP site certificate No. 1/182-1Drug-I-2024/10117, GMP (Revised Schedule M) and GLP certificates, manufacturing licences MLF252023HR000004 and MLF282023HR000005, ISO 9001:2015. Site master file and further certificates against the regulator’s requirement list.

Product documents

Specifications, method of analysis, batch manufacturing and packing records, certificates of analysis, and stability data from ICH accelerated and long-term studies in our own chambers.

Dossier support

Documentation in the format the target regulator uses, prepared with your registration agent, with queries from the assessor answered from the site.

With every consignment

Certificate of analysis, packing list, batch details and the shipping documents your customs and regulator require.

Packing for export

Language, artwork and shipping

Artwork and language
Cartons, labels and leaflets printed to your artwork in the regulator’s language. Blister and strip foil is printed inside the plant on our 4-colour rotogravure unit.
Primary packs
PVC and PVDC blister, alu-alu, aluminium strip, HDPE, PET and glass bottles, laminate tubes
Shippers
Export shippers with batch, expiry and consignee marking, palletised for container or air freight
Routes
Sea freight through Nhava Sheva (JNPT) or Mundra; air freight through Delhi. Terms and lead times are quoted per consignment.

How registration and supply run

Six steps from enquiry to repeat consignment

  1. Enquiry. Country, products, pack sizes, annual quantity and the regulator’s requirement list.
  2. Feasibility and proposal. Products checked against the export approvals and the licence; rate, batch size, lead time and documentation scope in writing.
  3. Dossier. Product and site documents prepared in the regulator’s format, with your registration agent.
  4. Registration. Assessor queries answered from the site; samples and stability updates supplied as asked.
  5. First consignment. Artwork approved, batch manufactured, released against specification and shipped with its certificates.
  6. Repeat supply. Consignments scheduled against your forecast, with stability commitments maintained for the market.

Questions importers ask

Before you send a requirement list

Which countries do you currently export to?

22 markets across Africa, Asia and Latin America: Nigeria, Ghana, Côte d’Ivoire, Benin, Mali, Burkina Faso, Kenya, Tanzania, Uganda, Ethiopia, Zimbabwe, Zambia, Cameroon, Nepal, Bhutan, Afghanistan, Uzbekistan, Tajikistan, Myanmar, the Philippines, Yemen and El Salvador.

Which products are approved for export?

39 export approvals are on the licence, written to USP and BP monographs: 34 tablets, 4 capsules and 1 oral suspension, across cardiovascular, anti-infective, gastro-intestinal, CNS and pain, anti-allergic and metabolic products. The full list is on the product list PDF.

Can you register a product that is not on the export list?

Yes. A new export approval is applied for from the Food and Drugs Administration, Haryana against a confirmed market and monograph, and the timeline is given with the proposal.

Which documents do you supply for registration?

Certificates of analysis, the WHO-GMP site certificate, GMP and GLP certificates, manufacturing licences, stability data and the documents on the importer’s registration requirement list. Certificate requirements differ by regulator and are agreed at the proposal stage.

Do you provide stability data for tropical markets?

Yes. ICH accelerated and long-term studies run in our own stability chambers, with conditions set to the climatic zone of the target market.

Can the pack be printed in our language?

Yes. Cartons, labels and shippers are printed to your artwork in the language the regulator requires, and blister and strip foil is printed inside the plant on our own rotogravure unit.

What is the minimum order for export?

It follows the batch size for the product, which comes with the proposal. Consignments are usually consolidated across products for a container or an air shipment.

Which port do you ship from?

Sea freight moves through Nhava Sheva (JNPT) or Mundra, and air freight through Delhi. Terms and lead times are quoted per consignment.

Talk to us about supply to your market

Send the country, the products, the pack sizes and the regulator’s requirement list. You will get feasibility, rate, lead time and the documentation scope in writing.

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info.vh@vibcare.co.in  ·  +91 85660 76607  ·  Khasra 6/2/2, Kot Road, Village Dabkori, Panchkula, Haryana 134103