Available Raw Materials & Active Pharmaceutical Ingredients

Lidocaine Base

Lidocaine Hydrochloride




Licorice Root Extract

Magnesium Ascorbate 20%

Magnesium Citrate 16%

Magnesium Chloride

Magnesium Oxide

Magnesium Sulfate


Milk Thistle Extract

Naladixic Acid Sodium Salt

Naphazoline Hydrochloride

Neem Oil

Neomycin Sulphate





Nitrovin Hydrochloride

Noscapine Base


Oxolinic Acid

Oxolinic Acid Sodium Salt


Oxymetazoline Hydrochloride

Oxyquinoline Sulphate

Oxytetracycline Hydrochloride



Penicillin G Procaine

Penicillin Potassium V & G

Podophyllum Resin

Potassium Acetate

Potassium Aluminum Sulphate

Potassium Bitartrate

Potassium Carbonate

Potassium Chloride

Potassium Citrate

Potassium Gluconate

Potassium Guaiacolsulfonate

Potassium Iodide

Potassium Phosphate Mono

Pramoxine Hydrochloride

Prednisolone + Salts




Procaine Hydrochloride

Psuedoephedrine HCL


Rhodiola Rosea 3%


Riboflavin 5 Phosphate Sodium

Riboflavin Tetrabutyrate



Saw Palmetto Berry Ext Power 25%

Saw Palmetto 45%

Saw Palmetto extract (CO2)

Silicon Dioxide

Sodium Sulfate


Tartaric Acid


Terbutaline Sulphate


Tetracycline Base & HCI

Theophylline Anhydrous

Theophylline Hydrous

Tribulus Terrestris Extract 40%

Tribulus Terrestris Extract 60%

Tribulus Terrestris Extract 80%

Urea Crystals

Vitamin B6 Multiple Forms

Vitamin B12 – Multiple Forms

Vitamin E Oil (Natural & Synthetic)

Vitamin E Powder (Natural & Synthetic)

Vitamin F

Vitamin K

Whey Protein 80%

Whey Protein 80% (Instantized)

Whey Protein 90% (Instantized)

White Willow Bark Extract

Yohimbe 2%

Yohimbinine Hydrochloride

Zinc Ascorbate

Zinc Sulphate Monohydrate

Quality and Standards:

We apply and adhere to a strict set of quality standards, and we have policies and procedures in place to identify, measure, control and sustain product-quality excellence. We continuously strive to improve these standards in order to enhance procedures and ensure ongoing compliance with current Good Manufacturing Practices (GMP).

All manufacturing facilities that Canadian National Pharma Group owns and operates, and any company from which we purchase formulated pharmaceuticals, active ingredients and sterile products, must comply with GMP. These standards include requirements for verifying the sources of incoming materials, and for the manufacturing, storage, handling and distribution of products.

Counterfeit products are a growing global problem and a serious threat to public health. We at Canadian National Pharma Group believe that maintaining the integrity of our supply chain is of paramount importance.

Supplier Selection:

Canadian National Pharma Group maintains strict quality standards no matter where in the world our products are manufactured. Once we have made a decision to engage an external manufacturer, that manufacturer is required to comply with Canadian National Pharma Groups’ business requirements set forth in the contract, regardless of geography.

We conduct audits of every potential new supplier of active pharmaceutical ingredients or formulated products and sterile products to determine its acceptability and compliance with GMP.

Audits and Inspections:

We conduct Quarterly audits to further ensure that suppliers continue to meet GMP. Through such audits, we evaluate the continued acceptability of the facility from a quality assurance and regulatory compliance perspective.

Quality tests are performed on all active pharmaceutical ingredients that Canadian National Pharma Group purchases as part of our overall supplier-qualification process, and further tests are performed during subsequent stages of manufacturing. Quality tests are performed on all formulated products before we release them to the marketplace.