The complete catalogue
Every API we make, and every way we can make yours
What you get from a direct manufacturer
Manufactured and tested under GMP and GLP certificates from the Gujarat FDCA.
Batch-wise CoA as standard; DMF and open-part dossiers available for filings.
Sample and R&D quantities through to repeat commercial tonnage.
Domestic despatch from Bharuch plus export documentation handled in-house.
Direct access to the people who release the batch, not an account manager.
Who we supply
Three kinds of buyer, one supply standard
Whether you are filing a dossier, filling a purchase order or scaling a generic, the documentation and batch consistency you receive is the same.
Consistent, documented API supply for oral solids, injectables and semi-solids — with the paperwork your QA team will ask for before the first PO.
Bulk quantities with export-ready documentation, stable pricing and packaging configured for onward shipment.
Small development quantities, impurity data and grade flexibility while your product is still in formulation trials.
Why Apex
You are buying from the plant, not from a trading desk
Apex Pharma API owns and operates its own manufacturing block at Saykha GIDC. That means the price you are quoted is the manufacturer's price, the batch record you receive is ours, and the person answering your technical query works in the same building as the reactor.
More about the company →No trading margin between the reactor and your purchase order.
Same route, same plant, same QC release protocol on every campaign.
CoA, MSDS and specification sheets issued without chasing.
Ten years of despatch documentation from a Gujarat GIDC estate.
Quality & compliance
What each certification means for your dossier
Your auditor sees controlled processes, trained operators and traceable batch records.
An in-house testing laboratory certified to GLP by the Gujarat FDCA.
A documented management system behind the deviation, change and CAPA process.
Capability snapshot
A single-site operation you can audit in a day
Flagship molecules
Our three most-documented, highest-volume APIs
Our highest-volume molecule, with the widest grade coverage and the fastest documentation turnaround.
Repeat annual contracts with formulators; micronised particle-size options available on request.
Tight impurity profile and full analytical data package for regulated filings.
Exporting to Pakistan, with supply available to non-regulated markets. Client logos and testimonials will be added as they are confirmed — nothing on this site is stated before it can be evidenced.
What is your minimum order quantity?
MOQ depends on the molecule and grade. For most of our eight APIs we supply from trial quantities upward, and we will confirm the exact MOQ against your specification when we quote.
Can you send a sample before we commit?
Yes. Working samples with a batch CoA are available for evaluation. Tell us the grade and quantity you need for your formulation trials.
What documentation do you provide?
Batch-wise Certificate of Analysis, MSDS, specification sheet and method of analysis as standard. DMF and open-part dossiers are available on request for regulatory filings.
What are your typical lead times?
Stocked grades despatch quickly; campaign-manufactured quantities are scheduled against your PO. We commit to a date at quotation stage rather than after the order.
Do you export outside India?
Yes. We handle export documentation in-house from our Bharuch plant. Share the destination market and we will confirm what is required for your import.
Looking for a reliable API manufacturing partner?
Send us the molecule, grade and indicative volume — you will get a quote and a documentation list back, not a sales call.