Therapy Areas Markets Capabilities Contact Grow

Indian generic pharmaceutical trading
WHO-GMP and PIC/S certified supply network
Registered in Southeast Asia, the Caucasus and Central Asia

Licensed merchant exporterIndia
One Star Export HouseMinistry of Commerce
Established1987

A shortlist for your
market, drawn from
2,186 molecules.

We work out what a market already registers, who supplies it today, and where the gaps sit. You get a filing order: the molecules to register first, and the dossier route behind each.

Know the market.
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Therapy areas

Three areas account for 998 of the 2,186 molecules in the range.

Every molecule here has technical documentation held with the plant. Name the market and compilation to your authority's format begins.

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Technical data at source
Anti-Infectives
473
molecules
Meropenem + Sulbactam 1.5g
Ceftazidime + Sulbactam 750mg / 1.5g / 3g
Caspofungin, Micafungin, Anidulafungin
Daptomycin 350 / 500mg
Sofosbuvir 400mg + Velpatasvir 100mg
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Cardiovascular
& Metabolic
344
molecules
Sacubitril + Valsartan (3 strengths)
Apixaban 2.5 / 5mg
Rivaroxaban 2.5 / 10 / 15 / 20mg
Empagliflozin 10 / 25mg
Dapagliflozin 5mg + Metformin SR 1000mg
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CNS /
Neuropsychiatry
181
molecules
Aripiprazole (six strengths)
Quetiapine 25 / 50 / 100 / 200mg
Duloxetine DR 30 / 60mg
Divalproex Sodium ER 750 / 1000mg
Pregabalin SR 75mg + Methylcobalamin 1500mcg
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Portfolio
2,186

Across eleven published therapy areas and five dosage forms

Active markets
4

Myanmar, Georgia, Turkmenistan, Tajikistan

Registrations in force
138

Cleared with the drug authorities of the four active export markets

Established
1987

One Star Export House, Ministry of Commerce, India

How we work

Every enquiry starts from what is already registered in the market.

The analysis runs before any shortlist goes out, so the conversation opens on molecules the market can register.

The same analysis sets the order we file our own dossiers in.

Market and competitor analysis
What your authority has already approved, and who is supplying against it.
Range cross-match
A ranked list of molecules, each with its dosage form and the certification behind it.
Documentation route
CTD dossier, COPP, and the plant-level WHO-GMP and PIC/S certificates.

Manufacturing

WHO-GMP and PIC/S certified supply across five dosage forms.

Oral Solids
Tablets & Capsules

Immediate and extended-release formulations across cardiovascular, diabetes, CNS and anti-infectives. Full ER and MR capability, including sustained-release combinations such as Pregabalin SR with Methylcobalamin and Divalproex Sodium ER. Dispersible tablets and dry syrups included.

WHO-GMP PIC/S
Parenterals
Dry & Liquid Injectables

Small-volume parenterals across the anti-infective spectrum: cephalosporins, carbapenems, reserve-class antibiotics, antifungals and corticosteroids. Lyophilised and liquid formats. Sterile manufacturing to BP and USP standards.

WHO-GMP PIC/S
Large-volume parenterals
IV Infusions

Sterile large-volume parenterals. Sodium chloride, dextrose, metronidazole, levofloxacin, paracetamol, and mannitol infusions. Glass and plastic containers. Terminally sterilised to WHO-GMP standard.

Large-volume parenterals require dedicated lines, separate from small-volume sterile filling. 12 molecules in the range, and the capability that opens institutional and hospital accounts.

WHO-GMP PIC/S
Specialist forms
Inhalers & Ophthalmics

Pressurised metered-dose inhalers, aqueous nasal sprays and sterile ophthalmic drops. MDI manufacture requires pressurised filling capability separate from standard sterile injectable lines. The ophthalmic range includes preservative-free presentations and combination antibiotic-steroid drops.

47 metered-dose inhalers, 30 nasal sprays and 177 ophthalmic presentations, together the 254 molecules on this card.

WHO-GMP PIC/S
Liquids & topicals
Syrups, Creams & Sachets
Syrups and dry syrups, dermatological creams and ointments, and sachet formats. Dry syrups ship as powder and are reconstituted at dispensing, which is how paediatric anti-infectives reach markets where a ready-made suspension would not hold its shelf life.

260 molecules, third after oral solids and injectables.
WHO-GMP PIC/S

Full dosage form breakdown under Capabilities.

Markets

138 registrations in force across four drug authorities.

Each one was filed with the authority of the market it covers. We hold nothing yet in the Middle East or Africa, which is where the next filings go.

Active markets
Myanmar in Southeast Asia, Georgia in the Caucasus, and Turkmenistan and Tajikistan in Central Asia. All four hold registrations in force.
138
Registrations
Expansion corridors
The Middle East and Africa. Sourcing plants hold accreditations from 14 of the 22 authorities behind them. Aravis holds no product registration in either region.
Not filed
No registrations

Every new supply relationship starts the same way, whether or not Aravis is already registered in the market. Request a portfolio analysis.

A gap analysis starts with your market and your current range.

Tell us the market and what you stock.

Start the conversation