Pharma Manufacturing Company for Sale in Uttarakhand – ₹10 Cr

Plot Size

14000 Sq. Ft.

Building Size

25000 Sq. Ft.

Asking Price

INR 10 crore

Available

For Sale

Certification

GMP

Company Details

Confidential listing · Roorkee, Haridwar district, Uttarakhand · Full sale

The short answer

A pharma manufacturing company for sale near Roorkee, in Haridwar district, Uttarakhand, offered together with its own marketing arm. The plant makes tablets and capsules (non-beta-lactam) and sits on the Delhi–Haridwar highway. The asking price is INR 10 crore against a declared annual turnover of INR 20 crore.

The seller declares about 14,000 sq ft of land and 25,000 sq ft built up, capacity of 10 lakh tablets and 5 lakh capsules per eight-hour shift, and a marketing network of more than 550 distributors and 600 running products. The drawing set also shows an ointment section, a sheet marked beta-lactam and a vacant upper floor. None of these are on the seller’s list of approved sections, so check them before you put a value on them.

Listing prepared by Laafon Galaxy Pharmaceuticals · Updated 13 October 2026

  • Asking priceINR 10 CrFull sale
  • Annual turnoverINR 20 CrSeller declared
  • Approved sections2: tablets, capsulesNon-beta-lactam
  • Land / built-up~14,000 / ~25,000 sq ftSeller declared
  • Capacity per shift10 lakh tab · 5 lakh capEight hours, seller declared
  • Marketing arm550+ distributors600+ running products

Verification level

  1. Seller declared
    13 Oct 2026
  2. Document reviewed
  3. Site inspected
  4. Independently verified

Sections, capacity, turnover, distributor numbers and areas come from the seller, the seller’s machine list and the seller’s drawing set. Laafon Galaxy has not yet reviewed licence copies or accounts, or inspected the site. Use this page to plan your document check and site visit.

What sits where in the building

The seller’s drawings show two floors with several levels. Select an area to see what is drawn there. Green areas are the approved sections the seller lists; amber areas are drawn but their licence status is not confirmed; grey areas are support space.

2approved sections (seller declared) 2drawn areas with licence status to confirm 4support or vacant areas

Approved (seller declared)Status to confirmSupport or vacant

Ask about the beta-lactam sheet before anything else. The revised Schedule M requires dedicated, self-contained facilities for highly sensitising products such as penicillins [1]. If a penicillin or cephalosporin product was ever made in those rooms, ask for the decontamination and residue-test records before you plan any other use for them [8].

The facility

Photographs supplied by the seller. Select an image to enlarge it.

  • The unit near RoorkeePhotograph supplied by the seller.
  • Second viewPhotograph supplied by the seller.

What you are buying

Licences and certificates, as declared

  • Drug manufacturing licences for tablets and capsules (non-beta-lactam), issued by the State Drug Licensing and Controlling Authority at Dehradun [5]. Licence copies, issue dates and retention-fee receipts have not yet been shared; since 2017 a licence stays valid on payment of a retention fee every five years [4].
  • Product permissions: the seller declares about 1,000 approved formulations.
  • GMP certificate: the seller describes the unit as GMP certified under the revised Schedule M. Read the certificate itself: one that does not name the revised schedule does not show compliance with it.
  • ISO 9001 quality management certificate, validity to be confirmed.
  • Wholesale drug licence: one site plan in the set marks the administration block for a wholesale drug licence. Confirm which company holds it.

Ask at diligence: the product permission list endorsed on each licence, whether the ointment section and the area on the beta-lactam sheet were ever endorsed, and the latest State inspection report against the revised Schedule M.

Deal maths at the asking price

Change the offer, the turnover or the margin to see the multiples. The turnover is seller declared; the margin is your own assumption until you have read the accounts.

Asking price is 10
Seller declared: 20
Your assumption
  • Price ÷ turnover0.50xTimes annual sales
  • Implied EBITDAINR 2.00 CrPer year, at your margin
  • Price ÷ EBITDA5.0xYears of EBITDA to recover the price

Before tax, interest, capital spending and working capital. A screening aid, not a valuation. To compare against building a new oral solid plant, use the plant setup cost calculator.

Revised Schedule M and the licences

The revised Schedule M was notified as G.S.R. 922(E) on 28 December 2023 [1]. Firms with turnover up to INR 250 crore that applied with an upgradation plan had until 31 December 2025 [2], and the Health Ministry signalled it would not extend again [9]. In November 2025 the Drugs Controller General asked every State to inspect units against the new standard and report monthly [3]. At a declared INR 20 crore turnover this unit is in that band, so the question for a buyer is not whether it must comply, but whether the State has inspected it and what was found.

Deal elementWhat happens
Share purchaseThe licensee company stays the same and the licences continue. Notify the Licensing Authority of the change in constitution; the licence then stays valid for up to three months unless a fresh licence is taken [6]. You inherit the company’s history, including past liabilities.
Asset purchaseThe licences stay with the seller. You need a fresh application, inspection and grant against the revised Schedule M, and production stops until they are granted.
Land in Haridwar districtIn a share purchase the land stays with the company. In an asset purchase it is a land sale. Uttarakhand’s 2025 amendment to its land law left Haridwar outside the bar on outsiders buying farmland, but moved approval of land sales there to the State government [7]. Check the notified text and the land’s recorded use with a local advocate.
Marketing companyA separate company. Its brands, distributor agreements and wholesale licence move only if its own shares, or the assets themselves, are part of the deal.

Scroll the table sideways on a phone.

Ten questions to put to this seller

  1. Licence copies with the endorsed product permission lists, issue dates and retention-fee receipts.
  2. The revised Schedule M gap assessment, whether an extension application was filed, and the latest State inspection report with its CAPA status.
  3. The beta-lactam sheet: was a beta-lactam section ever licensed or run, what the rooms are used for today, and the decontamination and residue-test records.
  4. The ointment section: licensed, idle or only planned.
  5. The title deed, the land’s recorded use, the latest sanctioned plan and the completion certificate for the full built-up area.
  6. The QC instrument list and the utilities list: air handling, purified water, compressed air and power backup.
  7. How the 10 lakh tablet and 5 lakh capsule capacity figures are calculated, with actual batches for the last 12 months.
  8. Three years of audited accounts for both companies, split between own brands and third-party work, matched to GST returns.
  9. For the marketing arm: whether it is in the deal, trademark registrations, distributor agreements, receivables and stock in the channel.
  10. Pollution Control Board consents (the drawings show an ETP), fire NOC, factory licence, and which key technical staff will stay.

For everything else, use our 50-point pharma plant acquisition checklist.

Deal terms and ideal buyer

This is a full sale of the manufacturing company with its land, building, machinery, licences and product permissions, offered together with its marketing arm. The asking price is INR 10 crore. Financials, licence copies and technical files are shared only after a mutual NDA.

Who it suits: a PCD or marketing company that wants its own oral solid plant; a buyer who wants a factory and a running distribution network in one transaction; a third-party manufacturer adding tablet and capsule capacity close to Delhi; or a group ready to complete the revised Schedule M work and use the vacant upper floor to grow.

Register interest in this Roorkee company

In your first message, send your company name, business model and how you plan to use the plant. Put Pharma Manufacturing-Marketing Company for Sale, Roorkee in the subject line.

Darshan Singh · Promoter representative
Email: contact@laafon.com
Phone / WhatsApp: 9812446733

Frequently asked questions

References

  1. Ministry of Health and Family Welfare. Drugs (Amendment) Rules, 2023 (revised Schedule M). G.S.R. 922(E), 28 December 2023. Premises requirements on dedicated facilities for sensitising products. Notified text (PDF). Accessed October 2026.
  2. Ministry of Health and Family Welfare. Drugs (Amendment) Rules, 2025: revised Schedule M deadline extended to 31 December 2025 for manufacturers with turnover up to INR 250 crore that applied with an upgradation plan. G.S.R. 127(E), 11 February 2025. Reported by Business Standard, 24 March 2025. Trade press.
  3. Press Trust of India. DCGI orders inspections of pharma units to ensure compliance with revised Schedule M norms. 10 November 2025. theweek.in. Trade press.
  4. Ministry of Health and Family Welfare. Drugs and Cosmetics (Tenth Amendment) Rules, 2017. G.S.R. 1337(E), 27 October 2017 (licence renewal replaced by a retention fee every five years). Summary on Mondaq. Accessed October 2026.
  5. Department of Medical Health and Family Welfare, Uttarakhand. Drug Control Administration: Drug Licensing and Controlling Authority, Dehradun. health.uk.gov.in. Accessed October 2026.
  6. Drugs and Cosmetics Rules, 1945. Form 25 (Rule 70) and Form 28 (Rule 76): licence conditions on change in the constitution of the firm. Specimen licence text (PDF). Accessed October 2026.
  7. Scroll. Uttarakhand Assembly clears bill to restrict outsiders from buying agricultural land. 22 February 2025. scroll.in. Trade press; check the notified Act.
  8. US Food and Drug Administration. Non-Penicillin Beta-Lactam Drugs: A CGMP Framework for Preventing Cross-Contamination. Guidance for Industry. fda.gov (PDF). International benchmark, not Indian law.
  9. Business Standard. Health ministry unlikely to extend Schedule M GMP deadline for MSME pharma. 29 December 2025. business-standard.com. Trade press.

This listing is commercial and technical information for prospective buyers. It is not investment, legal or tax advice, and it is not an offer. All figures are declared by the seller and have not been independently verified by Laafon Galaxy Pharmaceuticals. Check them against original documents and a physical inspection, and confirm the current regulatory position with the Drug Licensing and Controlling Authority, Uttarakhand, and your own advisers before committing funds.

Before you make an offer

Seller-declared information

Four things to confirm first

  1. Form 25 and Form 28 licence validity, and how the State Licensing Authority will handle the change of ownership.
  2. The Revised Schedule M gap assessment and what upgrades are still open.
  3. Land title or lease terms, and the approved building plan.
  4. Turnover and capacity figures, which stay seller-declared until documents are reviewed.
Plant acquisition checklist

Name, licence numbers and exact address are shared after an NDA.

Production Capacity: Tablet 10 Lakh and Capsules 5 Lakh per day /8 hours
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Pharma Manufacturing-Marketing Company for Sale
Pharma Manufacturing-Marketing Company for Sale