Pharmaceutical
manufacturing on Long Island.
We manufacture, test, package, and label pharmaceutical products. Every stage happens inside our own plant.
Helping improve the quality of life for people everywhere.
We make products people rely on, and we make them the same way every time. What ships is what the specification says it should be.
Seven divisions, integrated end to end.
Each stage feeds the next without leaving the building. Material never changes hands, and the record follows it the whole way.
Receiving
Intake, quarantine, and identity testing. Nothing reaches the floor unreleased.
Manufacturing
Actives and excipients weighed, blended, and granulated to batch parameters.
Production
Bulk becomes dose. Tablets compressed, capsules filled, coatings applied.
Testing
Assay, uniformity, and stability work — in-process and at final release.
Packaging
Bottling, blister, induction sealing, and cartoning under controlled conditions.
Labeling
Labels applied and vision-verified in line, coded to lot and expiry.
FDA Compliance
Contents and ingredient sources recorded per bottle, traceable to supplier lot.
Pharmaceutical Production
We currently produce more than 75 products. Our equipment holds weight, hardness, and content uniformity within specification across runs of any size, from ten thousand units to over a million.
Integrated pharmaceutical manufacturing.
We have manufactured OTC pharmaceutical products for over 30 years.
World class manufacturing.
AZ Pharma Labs operates a pharmaceutical plant in a special economic zone in Hauppauge, New York, on Long Island. Seven divisions run there, each feeding the next.
Our staff includes process engineers, production operators, and quality specialists, many of whom have worked in regulated manufacturing their entire careers.
Documented
Every batch has a written record, kept and retrievable for audit.
Tested On Site
Our laboratories are in the building, so testing is not sent out.
On Schedule
We plan production around delivery dates and meet them.
Regulatory record.
We have a long record of meeting and exceeding OTC regulatory requirements. Product is tested on arrival, during production, and again before release.
Nothing ships until those results clear.
Seven divisions, integrated.
Receiving, manufacturing and production, testing, packaging, labeling, and the FDA-required data management behind every unit — a record of what is in each pill in each bottle, and the source of every ingredient it contains, held for traceability. We also support FDA and other U.S. approvals for the production and sale of specific drugs.
Receiving
Raw materials and components arrive under scheduled intake, are quarantined on receipt, and are held until identity and quality are confirmed against specification.
Each lot is logged to its supplier on arrival. That record stays with the material through every stage that follows.
Manufacturing
Released material is weighed and dispensed to the batch record, then blended and granulated in validated vessels under controlled temperature and humidity.
Process parameters are recorded during the run.
Production
Bulk becomes finished dose. Tablets are compressed and capsules filled on high-output lines, with coating applied where the formulation calls for it.
Weight, hardness, and content uniformity are checked throughout the run and held within specification.
Testing
Material is tested on arrival, product is checked during production, and finished goods are released only after they meet full specification.
Our laboratories are on site, so testing does not have to be sent out and waited on.
Packaging
Finished dose is counted, filled, and sealed in controlled conditions built to guard against contamination and hold shelf life to its stated date.
Bottling, blister, induction sealing, and cartoning run as automated, high-throughput operations.
Labeling
Content, strength, lot number, and expiry date are printed and inspected as bottles run. Vision systems reject any label that does not scan correctly.
Artwork is version-controlled and checked against the batch record before the run starts.
FDA Compliance
Every unit produced here carries a data record behind it, maintained to FDA requirement and retained for the life of the product.
Any bottle can be traced back to its batch, to the raw material lots used, and to the suppliers that shipped them.
The same documentation supports approval work. We compile the manufacturing and analytical evidence behind FDA and other U.S. submissions required to produce and sell a specific drug.
All seven stages, one facility.
Because we run every stage ourselves, there are no outside handoffs to schedule around and no gaps in the production record.
Reach the plant.
Our office is open Monday through Friday, 8:00 AM to 5:00 PM Eastern. You can reach us by phone or email.