§1What this business is

Tablets are the most common form of medicine. The unit weighs out drug and excipient powders, blends and granulates them, dries the granules, presses tablets on a compression machine, coats them if needed and packs them in PVC-aluminium blister or strip packs. Each batch is tested by quality control. Buyers are pharma marketing companies (contract or third-party manufacturing), distributors and hospitals.

§2Is it right for you?

Who it is for

A pharmacy graduate or someone with pharma production experience and contacts with marketing companies.

Who it is not for

Someone without pharma knowledge — regulators expect technical staff and full records.

Advantages

  • Tablets are the most used form of medicine
  • Third-party manufacturing for marketing companies gives steady orders
  • Machine line is well known and locally made
  • Healthy DSCR (3.00) in the report

Drawbacks

  • Strict drug licence and GMP (Schedule M) rules
  • Needs a qualified pharmacist or chemist on staff
  • Quality failures can mean recalls and licence action
  • Large established units compete on price

Skills you need

  • Tablet formulation and process control
  • Quality control testing
  • GMP documentation (BMR, MFR)
  • Dealing with drug regulators and buyers

Why difficulty 4/5: Machines are standard, but drug licensing, GMP and quality control are demanding.

§3Market

Who buys

  • Pharma marketing companies (third-party manufacturing)
  • Distributors and stockists
  • Hospitals and government supply tenders

How it sells

  • Loan-licence and contract manufacturing
  • Own brand through distributors

Good to know

  • The report says about two-thirds of prescriptions are solid dosage forms, half of them compressed tablets.

§4Raw material & machinery

ItemQtyCost
Vibro sifter1₹75,000
Rapid mixer granulator1₹3,38,000
Tablet compression machine1₹3,50,000
cGMP fluid bed dryer1₹2,50,000
Cone blender1₹1,35,000
Coating pan1₹1,27,000
Packaging machine1₹2,29,500

From: PMEGP sample project report — Medicinal tablets (prepared by Udyami/Samadhan)

  • Active ingredients (APIs) and excipientschecked and released by quality control before use
  • PVC and aluminium foilfor blister and strip packing
  • Cartonssecondary packing

From: PMEGP sample project report — Medicinal tablets (prepared by Udyami/Samadhan)

§5Licences & registration

  1. Drug manufacturing licence from the State Drug Controller (FDA)
  2. GMP compliance (Schedule M)
  3. Udyam registration
  4. GST registration
  5. Fire NOC
  6. Pollution control board NOC

We can do this registration for you

§6Schemes & subsidies

PMEGP (the report is a PMEGP sample), CGTMSE for loans without collateral, and Stand-Up India for SC/ST and women founders.

§7Money

How the investment is worked out: Report: plant & machinery ₹15.05 lakh, furniture ₹0.75 lakh, other assets ₹1.00 lakh, working capital ₹5.67 lakh = ₹22.47 lakh (machinery price includes GST and transport). Premises rented.

Working capital: Working capital ₹5.67 lakh, of which working capital loan ₹5.10 lakh.

Year not printed on the report — check current machinery prices.

How to prepare a loan file

§8Export potential

Confirm the HS code in the DGFT ITC(HS) lookup before you export

3004Medicaments in measured doses or packed for retail sale

Export council / board: Pharmexcil

  • Confirm the 8-digit ITC(HS) line with DGFT or your customs broker.
  • You need an Import Export Code (IEC) from DGFT before the first shipment.
  • Export of medicines needs product registration in most buying countries.

§9Risks — where people fail

  • Licence suspension after a failed sample
  • API and excipient price swings
  • Delayed payments from marketing companies
  • Cost of meeting revised GMP norms

§1030 / 60 / 90-day plan

A general plan that applies to any business. A plan for this business will be added after research.

  1. Days 1–30: Visit a working medicinal tablets manufacturing unit unit, ask 10 buyers about price and quantity, and get quotations from 3 suppliers.
  2. Days 31–60: Udyam and the licences you need (Drug manufacturing licence from the State Drug Controller (FDA), GMP compliance (Schedule M)), a project report (DPR), and the scheme or loan file.
  3. Days 61–90: Space and machines, trial production, and first deliveries to 10 customers.

§11Who to connect with

Not verified yet

Associations, clusters and training institutes — the directory is being built. Connect

§12Watch

There is no episode on this business yet. Shows are coming soon on the Podcast page.

Want to start Medicinal Tablets Manufacturing Unit?

DPR, loan file or registration — ask us on WhatsApp.

Get a DPR / loan file made

Sources

  1. PMEGP sample project report — Medicinal tablets (prepared by Udyami/Samadhan)

Data review: 6 October 2026. Spotted a mistake? Report it. For information only — not legal or financial advice.