Ayurvedic & Nutraceutical Third Party Manufacturing Company India

US FDA-Registered Facility · Khandwa, India

Third-Party Ayurvedic & Nutraceutical Contract Manufacturer for U.S. Supplement Brands

US FDA RegisteredWHO-GMP CertifiedDSHEA-AlignedLow MOQ Pilot Runs

Shakumbhri Groups operates a US FDA-registered (Registration No. 12421917160), WHO-GMP certified manufacturing facility in Khandwa, India, producing private-label and bulk tablets, capsules, syrups, juices, sea buckthorn juice and shilajit resin for American D2C, Amazon and pharmacy-channel supplement brands.

20+Countries Exported To
500+Formulations Ready
15+Years Manufacturing
5M+Units Produced
Export to the United States

An FDA-Registered Partner for Scaling U.S. Supplement Brands

The U.S. dietary supplement market rewards brands that can move fast on trending ingredients while staying audit-ready. Shakumbhri Groups’ Khandwa facility is US FDA-registered and WHO-GMP certified, manufacturing under ISO 22000:2018, FSSAI and AYUSH standards — giving American brand owners a documented, traceable supply chain from the first pilot batch.

We work with D2C founders, Amazon sellers and pharmacy-channel brands on tablets, capsules, syrups, juices, and two of the fastest-growing categories in the U.S. wellness market right now: sea buckthorn juice and Himalayan shilajit resin.

Facility Snapshot

  • Location: Plot No. 7, Industrial Area, Indore Road, Khandwa, Madhya Pradesh, India
  • US FDA Facility Registration: No. 12421917160
  • Certifications: WHO-GMP, ISO 22000:2018, FSSAI, AYUSH, NABL, Kosher, Organic
  • Facility size: 50,000 sq. ft., unidirectional-flow, ISO Class 8 cleanroom
  • MOQ: pilot runs from as low as 500 units for new D2C brand partners
Why Manufacture With Us

Built for U.S. D2C & Retail Scale

01

US FDA-Registered Facility

Facility Registration No. 12421917160 supports import of dietary supplements, proteins and nutraceuticals into the U.S.

02

Pilot-to-Scale Manufacturing

Start with pilot runs as low as 500 units and scale to 100,000+ units monthly without switching manufacturers.

03

Trend-Ready R&D

In-house R&D team of 15+ scientists that can formulate and sample fast-moving categories like shilajit and sea buckthorn.

04

Amazon-Ready Documentation

COAs and stability data formatted to satisfy Amazon supplement listing requirements and retailer quality reviews.

Product Range

Manufactured & Export-Ready for the U.S. Market

80+ Formulations

Tablets

Film-coated, enteric-coated and effervescent tablets for immunity, joint care and general wellness.

65+ Formulations

Capsules

Gelatin and HPMC vegetarian capsules, built for D2C and Amazon supplement listings.

Liquid Format

Syrups & Tonics

Palatable herbal syrups and tonics with precise dosing for functional-beverage brands.

Trending Now

Sea Buckthorn Juice

Antioxidant-rich Himalayan sea buckthorn juice, private-labeled for the fast-growing U.S. functional-juice category.

Trending Now

Shilajit Resin

Purified, lab-tested Himalayan shilajit resin — one of the fastest-growing SKUs in U.S. men’s wellness and vitality retail.

Bulk & Sachet

Juices & Powders

Nutraceutical juice concentrates and functional powders formatted for reconstitution or ready-to-drink formats.

Documentation & Compliance

Everything Your U.S. Launch Needs

Every order for U.S. brands ships with a documentation package built around DSHEA labeling and import requirements.

Certificate of Analysis

Batch-specific COA covering identity, purity and microbiological testing for every production lot.

Stability & Shelf-Life Data

Accelerated stability testing (40°C/75% RH) to support Supplement Facts panel shelf-life claims.

DSHEA-Aligned Labeling Support

Label compliance review to help your Supplement Facts panel and claims align with FDA/DSHEA expectations.

How It Works

From Enquiry to U.S. Dispatch

1

Consultation

Share your product concept, target category and reference formula.

2

Formulation

Select from 500+ ready formulas or request custom R&D and sampling.

3

Pilot Batch

Approve a low-MOQ pilot run before committing to full-scale production.

4

Production

WHO-GMP batch manufacturing with in-process QC and full traceability.

5

Export Dispatch

Full documentation, freight booking and delivery to your U.S. warehouse or 3PL.

Frequently Asked Questions

Exporting to the United States

Is Shakumbhri Groups registered to export to the United States?

Yes. Our Khandwa manufacturing facility holds US FDA Facility Registration No. 12421917160, supporting the export of dietary supplements, proteins and nutraceuticals to the United States.

What is the minimum order quantity for U.S. brands?

We offer pilot runs as low as 500 units for new D2C and Amazon brand partners, scaling up to 10,000-50,000 units per SKU for tablets and capsules as your brand grows.

Can you help with DSHEA labeling and Supplement Facts panels?

We provide label compliance review and the underlying documentation – COAs and stability data – to help your Supplement Facts panel and claims align with FDA and DSHEA expectations. Final label approval rests with your compliance team or regulatory counsel.

Do you manufacture shilajit resin and sea buckthorn juice for U.S. brands?

Yes. Both are among our fastest-growing export categories to the U.S. market. We offer private-label and bulk manufacturing for shilajit resin and sea buckthorn juice, including sampling for new brand partners.

How long does production and shipping to the U.S. take?

Existing formulations typically take 2-4 weeks to produce, plus 1-2 weeks for export documentation. Ocean freight to U.S. West or East Coast ports generally adds 3-5 weeks depending on the route.

Can you scale production as our brand grows?

Yes. Partners have scaled from 500-unit pilot runs to over 100,000 units monthly across multiple SKUs without switching manufacturers, while maintaining consistent WHO-GMP quality control.

Get a Free Manufacturing Quote

Start Your U.S. Manufacturing Partnership

Tell us about your target category and goals. Our export team typically responds within 24–48 hours with MOQ, pricing and timeline.

  • US FDA-registered, WHO-GMP manufacturing
  • Free consultation & feasibility assessment
  • Pilot runs from 500 units
  • DSHEA-aligned labeling support
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Get in Touch With Us

Takes under a minute — our team responds within 5 minutes

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Ready to Launch Your U.S. Supplement Brand?

Talk to our export team directly — WhatsApp response typically within minutes during business hours.

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