Third-Party Pharma Manufacturing in Himachal Pradesh
Glauben Pharma offers third-party pharma manufacturing in Himachal Pradesh for marketing companies across India. We make non-beta-lactam tablets, capsules and liquid orals under your brand at our licensed plant in Tahliwal, District Una. This page sets out what we make, how an order runs, what you need to send and who is responsible for what.
- LicencesForm 25 and Form 28, Drugs Rules, 1945
- Dosage formsTablets, capsules, liquid orals (non-beta-lactam)
- Lead timeTypically 30 days after artwork approval
- Advance25% of the proforma invoice
What we can manufacture for your brand
We manufacture only compositions covered by our approved product permissions. Check the product permission list or ask us about a specific molecule and strength.
| Category | What it covers | Available |
|---|---|---|
| Tablets | Uncoated, film-coated and enteric-coated (gastro-resistant) tablets | Yes |
| Capsules | Hard gelatin capsules, including pellet-filled combinations such as PPI (EC) with domperidone or levosulpiride (SR) | Yes |
| Liquid orals | Syrups, suspensions and oral drops | Yes |
| Beta-lactams | Penicillins (e.g. amoxycillin, amoxycillin-clavulanate) and cephalosporins (e.g. cefixime) need a dedicated, segregated facility | No |
| New FDCs | A combination not approved in India before is a new drug under the New Drugs and Clinical Trials Rules, 2019 and needs CDSCO approval first | Not without approval |
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Browse ready compositions in the product catalogue.
How a third-party order runs, step by step
- Enquiry and feasibilityShare the composition, strength, pack and quantity. We check it against our product permissions and production lines.Day 0
- Proforma invoice and agreementWe issue a proforma invoice and the third-party manufacturing agreement for signature.
- Purchase order and documentsSend the PO on your letterhead (brand name, packing, quantity, rate, MRP) with a copy of your drug licence by email.
- Advance paymentTransfer 25% of the proforma invoice amount to our bank account.
- Artwork approvalWe send the carton, label and leaflet designs. We revise them until you approve in writing.Lead time starts here
- Manufacturing and QC releaseThe batch is made to the approved master formula, tested by Quality Control and released by Quality Assurance.
- DispatchGoods are dispatched with the invoice and the batch certificate of analysis, typically about 30 days after artwork approval.About Day 30
Check you are ready and estimate your dispatch date
Order readiness checklist
Tick what you already have. Missing items are added to your enquiry message below.
Dispatch date estimator
Lead time starts once the artwork is approved and the advance is received.
This is an estimate, not a commitment. The confirmed date is given in your proforma invoice and depends on material availability, batch size and the production schedule.
Manufacturer and marketer responsibilities
The marketer shares responsibility for the product with the manufacturer under the Drugs Rules, 1945. The usual split is set out below; the signed agreement governs.
| Area | Glauben Pharma (manufacturer) | Your company (marketer) |
|---|---|---|
| Licences | Manufacturing licence and product permission for the composition | Wholesale drug licence, GST registration |
| Brand and artwork | Prepares designs to the approved composition and labelling format | Brand name, trademark, final artwork approval |
| Pricing | Quotes the manufacturing rate | Fixes the MRP, within the NPPA ceiling for scheduled formulations |
| Materials and production | Sourcing, testing of raw and packing materials, manufacturing to the batch record | — |
| Quality release | QC testing, QA batch release, certificate of analysis, retained samples | Checks the documents on receipt |
| Market | Supports investigations with batch records | Distribution, complaint intake, recalls with the manufacturer |
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Revised Schedule M is now being enforced
Revised Schedule M (G.S.R. 3(E), notified 28 December 2023) is the GMP standard Indian plants are inspected against. The extended deadline for MSME manufacturers ended on 31 December 2025, and state and central inspections are now under way. Because the marketer shares responsibility for the product, your manufacturer’s compliance matters to you.
- Pharmaceutical quality systemQuality manual and documented procedures
- Quality risk managementRisk-based decisions on process and change
- Change controlEvery change assessed before it is made
- Deviation and CAPARoot-cause analysis with corrective action
- Product quality reviewPeriodic trend review of each product
- Data integrityAttributable, legible, contemporaneous records
Copies of our manufacturing licences and the product permission list are shared with prospective partners on request.
What decides your manufacturing rate
Rates are quoted per product after the feasibility check. These are the main drivers:
Composition
- API cost and strength
- Number of actives
- Coating or pellets
Quantity
- Batch size
- Repeat versus one-off order
Packing
- Blister, Alu-Alu, strip or bottle
- Carton, label and leaflet printing
Taxes and market
- GST on the invoice
- Current input prices on the quotation date
Send your third-party manufacturing enquiry
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A written quotation is issued only after the feasibility check. Rates depend on composition, quantity, packing and current input prices.
Third-party manufacturing FAQs
How long does a third-party order take?
Typically about 30 days from artwork approval, once the 25% advance has been received. The confirmed date is given in the proforma invoice.
How much advance do you take?
25% of the proforma invoice amount, paid to our bank account after the agreement and purchase order are in place.
Which documents do I need to send?
A purchase order on your letterhead with brand name, packing, quantity, rate and MRP; a copy of your drug licence; and the signed third-party manufacturing agreement.
Do you manufacture beta-lactam products such as amoxycillin or cefixime?
No. Penicillins and cephalosporins need a dedicated, segregated facility. Our plant makes non-beta-lactam tablets, capsules and liquid orals.
Can you make a composition that is not on your list?
Only if it is covered by a product permission on our licence. A fixed-dose combination that has not been approved in India before is a new drug under the New Drugs and Clinical Trials Rules, 2019 and needs CDSCO approval first.
Who decides the MRP?
The marketing company fixes the MRP. For scheduled formulations under the Drugs (Prices Control) Order, 2013, it must not exceed the ceiling price notified by NPPA.
Where is the plant and what licences does it hold?
Plot No. 55, Phase III, Industrial Area, Tahliwal, District Una, Himachal Pradesh 174507. The plant holds drug manufacturing licences in Form 25 and Form 28 under the Drugs Rules, 1945.
Third-party manufacturing desk
- Plant
- Plot No. 55, Phase III, Industrial Area, Tahliwal, District Una, Himachal Pradesh 174507
- Phone / WhatsApp
- +91 98123 46283
+91 74047 01264