Iron Folic Acid Tablets Manufacturer India

What We Manufacture

Iron + Folic Acid Tablet — specifications & clinical context

Product Specifications

Generic Name	Ferrous Sulphate / Ferrous Ascorbate / Iron Polymaltose Complex + Folic Acid
Strength / Dosage	Multiple formulations — standard, high-dose, combination
Dosage Form	Film-Coated Tablet
Route of Administration	Oral
Pack Size	Strip of 10 · Bottle of 100 · 1000
Packaging	Alu-PVC blister · HDPE bottle
Storage	Store below 25°C · Protect from moisture
Shelf Life	24 months
Manufacturing Facility	WHO-GMP Certified · Birkoni, Chhattisgarh
Regulatory Status	DCGI Approved · Manufacturing Licence Held
Available For	Contract manufacturing · Third-party manufacturing · Direct institutional supply

Clinical Context

Iron + Folic Acid tablets are on the WHO Essential Medicines List and are the single highest-volume tablet procurement in India’s government health system — procured in billions of units annually through the Anaemia Mukt Bharat programme, NHM maternal health, ICDS and school health initiatives. Every pregnant woman in India is prescribed Iron + Folic Acid throughout pregnancy. Critical in export markets — anaemia affects over 50% of women and children across Sub-Saharan Africa and South Asia.

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Why 9M India

How Iron + Folic Acid Tablet is manufactured at 9M India

WHO-GMP certified manufacturing process

Ferrous Sulphate tablets require careful formulation — iron tablets can oxidise if not properly stabilised with antioxidants (ascorbic acid, sodium metabisulphite). Film-coating is essential to mask the metallic taste and prevent oxidation. IPC formulations are more stable and better tolerated — 9M India manufactures all three iron salt formulations. Stability testing under Zone IVa conditions validates product performance throughout shelf life.
In-house QC release testing — every batch

Iron content by AAS or HPLC · Folic Acid content by HPLC · Dissolution of both components · Content uniformity · Tablet disintegration · Microbial limits — all in-house.
Complete documentation within 24 hours

Manufacturing Licence · DCGI approvals · WHO-GMP Certificate · COA · COC · Stability data — pre-prepared, available within 24 hours.