Therapy Areas Markets Capabilities Contact Grow

Indian generic pharmaceutical trading
WHO-GMP and PIC/S certified supply network
Active in Southeast Asia and CIS — expanding to Middle East

Licensed merchant exporterIndia
One Star Export HouseMinistry of Commerce
Established1987

Your next supply partner
already knows
your market.

While others arrive with a catalogue, Aravis arrives having mapped your market, identified portfolio gaps, and prepared documentation-ready proposals — before the first conversation.

Know the market.
Grow Scroll to explore

The gap between what a market needs and what it receives is a sourcing problem. Aravis solves it before it becomes one.

Therapy areas

Three lead areas. Documentation depth across each.

Every molecule we propose is backed by technical documentation compiled to the regulatory standard of your market — the filing work is done before the commercial conversation begins.

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Registered
Documentation ready
Under registration
Anti‑Infectives
384+
molecules
Meropenem + Sulbactam / Tazobactam
Colistimethate Sodium 1 – 4.5 MIU
Sofosbuvir + Velpatasvir (HCV)
Ceftriaxone + Sulbactam / Tazobactam
Voriconazole 200mg
View portfolio →
Cardiovascular
& Metabolic
273+
molecules
Sacubitril + Valsartan (3 strengths)
Empagliflozin 10 / 25mg
Telmisartan + Amlodipine + HCT
Dapagliflozin + Metformin SR
Ticagrelor 60 / 90mg
View portfolio →
CNS /
Neuropsychiatry
160+
molecules
Pregabalin SR + Methylcobalamin
Levetiracetam 250 – 1000mg
Divalproex Sodium ER 250 – 1000mg
Risperidone 2 / 3 / 4mg
Citicoline 500mg
View portfolio →
Portfolio
817+

Molecules across Anti-Infectives, Cardiovascular & Metabolic, and CNS

Active markets
4

Myanmar, Georgia, Turkmenistan, Tajikistan

Active filings
138+

Registered across active markets — 400+ in documentation review

Established
1987

One Star Export House, Ministry of Commerce, India

How we work

The work happens before the meeting.

Most trading companies treat the first distributor conversation as the starting point. Aravis treats it as the midpoint. The market analysis, the gap identification, the documentation review — that work is complete before we pick up the phone. This is not a sales advantage. It is an operational discipline. And it is the reason distributors who engage with us move to commercial terms faster than with any other supplier.

Understand the market
Before any conversation, we analyse what your target market actually needs — which molecules are moving, where the supply gaps are, and which therapy areas represent viable commercial opportunity. Market intelligence precedes market entry.
Identify the gap
We match the market need against our portfolio. What you receive is not a full catalogue — it is a shortlist of molecules that are genuinely relevant to your market, with supply status and regulatory positioning for each.
Deliver documentation-ready proposals
The underlying technical documentation for every molecule we propose already exists. Regulatory submissions are compiled to the standard of your specific market authority. The filing process moves quickly because the substance of the work is already done.

Manufacturing

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

Tablets & Capsules
Oral Solids

Immediate and extended-release formulations across cardiovascular, diabetes, CNS, and anti-infectives. Full ER / MR capability including sustained-release combinations — Pregabalin SR + Methylcobalamin, Metoprolol Succinate ER, Divalproex Sodium ER. Dispersible tablets and dry syrups included.

WHO-GMP PIC/S
Dry & Liquid Injectables
Parenterals

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

WHO-GMP PIC/S
IV Infusions
Rare capability

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

Most Indian generic trading companies cannot source IV infusions competitively. This capability opens institutional and hospital accounts that other suppliers cannot reach.

WHO-GMP PIC/S
Inhalers & Ophthalmics
Specialist forms

Pressurised metered-dose inhalers, aqueous nasal sprays, and sterile ophthalmic drops. MDI manufacturing requires specialist pressurised filling capability — separate from standard sterile injectable lines. Ophthalmic range includes preservative-free formulations and combination antibiotic-steroid drops.

47 MDI and nasal spray molecules. 175 ophthalmic molecules across glaucoma, anti-infective, anti-inflammatory, and lubricant categories.

WHO-GMP PIC/S

Markets

Active markets. Honest about where we are.

We operate in markets where we have named distribution partners, active registrations, and filed dossiers. We do not list markets we are exploring as markets we are in.

Southeast Asia & CIS
Myanmar, Georgia, Turkmenistan, Tajikistan. Active registrations across all four markets. Established distribution partners. Ongoing regulatory submissions.
138+
Registered SKUs
Expansion corridors
Active exploration of select Middle East and African markets. Conversations underway. We will list these as active markets when registrations are filed.
In progress
No SKUs claimed

We are selective about where we expand. New market entries follow the same preparedness methodology as our current markets — analysis first, registrations second, distribution partnerships third. If you represent a distributor or importer in a market we have not yet entered, we are open to the conversation.

We are selective about
who we work with.
So are you.

Tell us your target market and what you import. We will assess whether our portfolio is a genuine fit — and come back with a molecule gap analysis if it is.

We respond to enquiries from registered importers, licensed distributors, and pharmacy chains with demonstrated market presence. Volume and regulatory context help us respond meaningfully.

We review all enquiries and respond within 48 hours where there is portfolio fit.