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Anti-bacterials

Amikacin Injection

100 mg/2 mL / 250 mg/2 mL / 500 mg/2 mL

Injection

2 mL Vial

Azithromycin Capsules

250 mg

Capsule

Azithromycin for Oral Suspension

100 mg/5 mL / 200 mg/5 mL

Dry syrup

Azithromycin Injection IP/USP

500 mg

Injection

Azithromycin Tablets

100 mg / 250 mg / 500 mg

Tablet

Chloramphenicol Capsules

250 mg

Capsule

Chloramphenicol for Oral Suspension

125 mg/5 mL

Dry syrup

Chloramphenicol Sodium Succinate Injection

1 g

Injection

Ciprofloxacin & Tinidazole Tablets

500 mg + 600 mg

Tablet

Ciprofloxacin for Oral Suspension

125 mg/5 mL / 250 mg/5 mL

Dry syrup

Ciprofloxacin Tablets

250 mg / 500 mg / 750 mg

Tablet

Clarithromycin for Infusion BP

500 mg

Injection

20 mL

Clarithromycin Oral Suspension

125 mg/5 mL / 250 mg/5 mL

Oral suspension

Clarithromycin Tablets

250 mg / 500 mg

Tablet

Clindamycin Capsules

150 mg / 300 mg

Capsule

Clindamycin Injection

300 mg / 600 mg

Injection

2 mL / 4 mL Ampoule

Co-trimoxazole Oral Suspension

40 mg + 200 mg

Oral suspension

Co-trimoxazole Tablets

960 mg

Tablet

Colistimethate Sodium Injection IP/BP

1 / 2 / 3 / 4.5 / 9 MIU

Injection

10 mL Vial

Daptomycin for Injection

350 mg / 500 mg

Injection

10 mL

Doxycycline Capsules

100 mg

Capsule

Doxycycline Hyclate & Lactic Acid Bacillus Capsules

100 mg + 60 Million spores

Capsule

Doxycycline Injection

100 mg / 200 mg

Injection

10 mL

Erythromycin for Oral Suspension

125 mg/5 mL / 250 mg/5 mL

Dry syrup

Erythromycin Lactobionate Injection

500 mg

Injection

Erythromycin Stearate Tablets

250 mg / 500 mg

Tablet

Fosfomycin Sodium for Injection

4 g

Injection

50 mL

Gentamicin Sulphate Injection

20 mg/2 mL / 80 mg/2 mL

Injection

2 mL Ampoule / Vial

Kanamycin Injection

500 mg / 1 g

Injection

Levofloxacin & Ornidazole Tablets

250 mg + 500 mg

Tablet

Levofloxacin & Tinidazole Tablets

500 mg + 500 mg

Tablet

Levofloxacin Syrup

125 mg per 5 mL

Syrup

Levofloxacin Tablets

250 mg / 500 mg / 750 mg

Tablet

Lincomycin Injection

600 mg/2 mL

Injection

2 mL Vial

Linezolid Tablets

600 mg

Tablet

Lymecycline Capsules

300 mg

Capsule

Metronidazole & Norfloxacin Suspension

100 mg + 100 mg/5 mL

Oral suspension

Metronidazole & Ofloxacin Suspension

100 mg + 50 mg / 200 mg + 100 mg

Oral suspension

Minocycline for Injection USP

100 mg

Injection

10 mL

Moxifloxacin Tablets

400 mg

Tablet

Netilmicin Sulphate Injection

50 mg / 100 mg / 200 mg / 300 mg

Injection

2 mL / 3 mL Ampoule

Norfloxacin & Metronidazole Tablets

200 mg + 200 mg

Tablet

Norfloxacin Tablets

400 mg

Tablet

Ofloxacin & Ornidazole Suspension

50 mg + 125 mg/5 mL

Oral suspension

Ofloxacin & Ornidazole Tablets

200 mg + 500 mg

Tablet

Ofloxacin & Tinidazole Suspension

50 mg + 100 mg

Oral suspension

Ofloxacin & Tinidazole Tablets

200 mg + 600 mg

Tablet

Ofloxacin for Oral Suspension

50 mg / 100 mg

Dry syrup

Ofloxacin Tablets

200 mg / 400 mg

Tablet

Polymyxin B for Injection USP

500,000 IU / 750,000 IU

Injection

10 mL Vial

Rifaximin Oral Suspension

100 mg/5 mL

Oral suspension

Rifaximin Tablets

200 mg / 400 mg

Tablet

Roxithromycin Oral Suspension

50 mg/5 mL

Oral suspension

Spectinomycin Injection

2 g

Injection

Streptomycin Sulphate Injection

750 mg / 1 g

Injection

Sulphamethoxazole & Trimethoprim for Oral Suspension

200 mg + 40 mg/5 mL

Dry syrup

Teicoplanin for Injection

200 mg / 400 mg

Injection

10 mL

Tigecycline for Injection IP/USP

50 mg / 100 mg

Injection

10 mL

Tinidazole Tablets

500 mg

Tablet

Tobramycin Sulphate Injection

40 mg/mL / 10 mg/mL

Injection

2 mL Vial / 5 mL Ampoule

Vancomycin Injection

250 mg / 500 mg / 1000 mg

Injection

20 mL

Need a strength or pack that is not listed? Ask us.

More In Pharmaceuticals

Healthcare products. Built for markets.

Tell Us What Your Market Needs.

Send the products and quantities you are looking for. We reply to every enquiry.

Send an enquiry rishabh@ripharma.in amit@ripharma.in

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FAQ

Frequently Asked Questions

How do you work with importers seeking distribution rights for Ripharma brands?

We partner with qualified importers and distributors to grow our brands in their markets. Each opportunity is assessed on territory, market potential, product range and the distributor’s commercial strength. Depending on the fit, we offer exclusive or non-exclusive rights, with territory, terms and performance targets agreed upfront.

Can you supply products under our own brand?

Yes. We can develop and supply products under your brand name, covering product selection, formulation and packaging, brand development, regulatory documentation and manufacturing coordination. Feasibility, minimum order quantities, development costs and regulatory needs are assessed for each product.

Are there minimum annual purchase commitments?

There is no fixed minimum. Commitments depend on the partnership, product range, territory, market potential and whether the products are Ripharma brands or your own. Any purchase commitments or sales targets are agreed before the partnership begins.

Who pays for dossiers, samples and registration?

This is agreed before each project starts. Depending on the product and country, costs can include dossier preparation, sample manufacturing and shipping, analytical testing, comparative dissolution or bioequivalence studies, and registration fees.

We ask for an upfront deposit to confirm your commitment before registration work begins. Costs may be shared, or one party may take a larger share, depending on the opportunity. All costs, deposits and payment milestones are documented before work starts.

Can the deposit be adjusted against future orders?

Yes. The deposit can be credited against your commercial orders over time, at an agreed amount or percentage per invoice. You recover the deposit through your purchases, and we gain confidence that registered products will reach the market.

What happens if registration fails, or no orders follow approval?

Both cases are covered by the Product Registration and Commercialisation Agreement signed before the project starts.

If registration fails, costs incurred and any unused deposit are settled under the agreed terms, taking into account why the application failed.
If registration succeeds but no orders follow within the agreed period, the agreement’s terms on registration costs, the deposit, reimbursement and territory rights apply.

This gives both sides clarity from the outset.

Who owns the registration and regulatory documents?

Ownership is agreed and documented before registration begins. It can differ for Ripharma brands and your own brands, and depends on the importing country’s rules. The agreement covers registration ownership, brand rights, access to documents and any transfer rights.

Do you provide marketing support?

Yes. Depending on the products and agreement, we can provide:

Product catalogues and information sheets
Brochures and promotional literature
Visual aids and presentations
Product images and approved pack artwork
Brand guidelines and approved marketing assets

For Ripharma brands, existing approved materials are available for your market. For private-label products, we can create custom materials, including design, adaptation, translation and artwork, under separate agreed fees.

Local marketing activity and its costs are the distributor’s responsibility unless agreed otherwise in writing. Materials must follow local advertising and regulatory rules, and any change to Ripharma brand assets needs our written approval.

Can you supply products that aren’t on your product list?

Yes. Through our manufacturing partners, we can source existing formulations or develop new ones, subject to feasibility. Each request is assessed on availability, manufacturing capability, regulatory needs, MOQs and commercial viability. Specifications, branding, pricing and timelines are agreed before we proceed.

How are quality complaints handled?

We work with the manufacturing partner’s quality team to investigate every reported complaint, deviation or non-conformity. Each case is documented and assessed under our quality procedures. Where needed, the root cause is identified and corrective and preventive actions (CAPA) are put in place. We keep you informed of progress and findings throughout.

Can we audit the manufacturing facilities?

Yes. With advance notice, and subject to the manufacturer’s approval, policies and confidentiality terms, we can arrange audits for you or your authorised representative. Scope, scheduling, documents and costs are agreed in advance.

Can multiple products ship together?

Yes, where possible we combine products into a single shipment to simplify logistics and reduce freight costs. This depends on product readiness, production schedules, storage and handling needs, documentation and regulatory requirements.

What are typical manufacturing and supply timelines?

Timelines depend on the product, packaging, order quantity, raw material availability and the manufacturer’s schedule. New developments need extra time for formulation, validation, testing and regulatory work. We confirm an estimated timeline with each quotation and order confirmation.

Still have a question?