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At 9M India Limited, trust through quality, transparency, performance.
About Granules & Powders
9M India manufactures pharmaceutical granules and oral powders from a WHO-GMP certified
facility in Birkoni, Chhattisgarh. Our granules and powders portfolio covers dry granules for
direct oral use, effervescent granules for solution preparation, and reconstitutable oral powders
— across nutritional, antibiotic, analgesic and gastrointestinal therapeutic categories.

Granule manufacturing at 9M India utilises wet granulation, dry granulation and fluid bed granulation technologies — with particle size distribution, bulk density, flow properties and dissolution characteristics validated at production scale. Oral powder formulations are manufactured with attention to blend uniformity, particle size and moisture content as critical quality attributes.
Every granule and powder formulation carries a valid DCGI manufacturing licence and is backed by complete regulatory documentation. In-house QC testing covers particle size analysis, blend uniformity, dissolution/disintegration for granules intended for oral use, and microbial limits testing before batch release.
Our Capabilities
From raw material blending and granulation through particle sizing, drying and final sachet or bulk filling — our granule and powder manufacturing covers every production stage under one WHO-GMP certified roof.
01
9M India employs wet granulation with high-shear mixers for formulations requiring improved compressibility and content uniformity. Dry granulation via roller compaction for moisture-sensitive APIs and formulations requiring low moisture content. Fluid bed granulation for superior flow properties and enhanced dissolution. Technology selection is based on API characteristics, target particle size distribution and intended use (direct oral granules, reconstitution or downstream compression).
02
Effervescent granules are manufactured under controlled low-humidity conditions to prevent premature reaction between acid and carbonate components. Critical manufacturing parameters include blend uniformity of effervescent components, moisture content, effervescence time and pH of resultant solution. Packaging in moisture-proof sachets or foil- laminate pouches is conducted in humidity-controlled environments. Effervescent formulations are particularly relevant for paediatric, geriatric and institutional oral dosing applications.
03
Oral powder formulations for direct consumption or reconstitution — including antacid powders, oral rehydration formulations, nutritional supplement powders and antibiotic dry powders for reconstitution into oral suspension. Blend uniformity is monitored as a critical quality attribute with stratified sampling protocols. Final moisture content and microbial limits are tested on every batch before release.
04
Granule and powder formulations are packaged in unit-dose sachets (foil laminate, paper- PE), multi-dose bottles (glass and HDPE) and bulk pack formats for institutional supply. Sachet fill weight accuracy is monitored with in-process checkweighing. Packaging line validation includes leak testing and hermetic seal integrity confirmation.
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All granule and powder formulations are supported by complete documentation — Manufacturing Licence, DCGI approvals, WHO-GMP Certificate, COA, COC, particle size data, blend uniformity records, stability data and product dossiers. Technical bid support for institutional tender submissions is available as standard.
Therapeutic Categories
Nutritional Supplements
Antibiotics
Gastrointestinal
Analgesics & Antipyretics
Respiratory
Why Choose Us
9M India stands out for its commitment to quality, precision, and innovation in tablet manufacturing. Our production facilities, regulatory compliance, and skilled teams ensure consistently reliable outcomes. We focus on delivering safe, effective, and high-performance formulations tailored to therapeutic needs, making us a trusted partner for brands seeking dependable pharmaceutical manufacturing excellence.
Wet granulation, dry granulation and fluid bed granulation — technology selected based on your API profile, not manufacturing convenience. Each process validated at commercial scale.
Effervescent granules require strict humidity control throughout manufacturing and packaging. Our facility maintains the environmental controls required for reliable effervescent granule production — not achievable in a standard oral solid manufacturing environment.
Unit-dose sachets, multi-dose bottles and bulk institutional packs — configured to your distribution channel, with fill weight accuracy and moisture-proof seal integrity validated on every packaging run.
Our Granules & Powders Range
ORS Powder | Nutritional | Sachet | Oral rehydration solution
Zinc Granules | Nutritional | Sachet | Mineral supplement
Paracetamol Effervescent | Analgesic | Sachet | Non-opioid analgesic
Acetylcysteine | Respiratory | Sachet | Mucolytic
Isabgol Husk | Gastrointestinal | Sachet / Bottle | Laxative
Amoxicillin Granules | Antibiotic | Sachet | Penicillin
Multivitamin Granules | Nutritional | Sachet | Vitamin supplement
Antacid Powder | Gastrointestinal | Sachet / Bottle | Antacid
We keep answer short
01
9M India manufactures dry granules for direct oral use, effervescent granules for solution preparation, and reconstitutable oral powders — including antibiotic dry granules, nutritional supplement sachets, effervescent analgesic granules and antacid powders.
02
Yes. Effervescent granules are manufactured under controlled low-humidity conditions with validated blend uniformity of effervescent components, moisture content monitoring and hermetically sealed sachet packaging.
03
Unit-dose sachets (foil laminate, paper-PE), multi-dose bottles (glass and HDPE) and bulk institutional packs. Sachet fill weight accuracy and seal integrity are validated on every packaging run.
04
Yes. Our granule and powder formulations are DCGI-approved and documentation is pre- prepared for institutional tender submission including state programmes and NHM supply.
05
Testing covers particle size distribution, blend uniformity, moisture content, dissolution/disintegration (where applicable), assay and microbial limits. COA issued from our in-house QC laboratory on every batch.
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