Name of active  ingredient 
:

  •  Please refer Appendix 8 List of Ingredients (active) Not Allowed to be Registered by the Drug Control Authority. 
  • The Active Pharmaceutical Ingredient(API) that is employed in the manufacturing process shall be named. For example:
    •  Where the API used is the salt (e.g. ampicillin trihydrate) which will yield an equivalent effective component from its base content (i.e. ampicillin), the substance name is the salt and the equivalent base component should be indicated in the respective columns.
    • Similarly where a chemical is a component in the ingredient, the component/elemental details (e.g. iron in ferrous sulfate) shall be stated in the remarks field if a label claim of the component is made for the product.ns for the product.
  •  International Non-proprietary Names (INN), approved names, pharmacopoeia names of ingredients shall be used whenever possible.
  • After each ingredient entry is correctly made, click the button ‘add/ save’. The button ‘remove’ will allow for corrections to an entry under this heading. To remove item, please select item from the listing and click ‘remove’.

Strength of active  ingredient :

  •  Please enter strength of active ingredient (numerical) and then select unit weights and measures from the drop-down list.
  • Content of ingredients shall be expressed as appropriate in the following manner:
    • quantity per dose unit(e.g. for unit dose formulations – tablet, capsule, lozenge, etc.)
    • percentage composition - %w/w, %w/v, %v/v, etc.(e.g. for products without defined dose unit such as ointments, creams, solutions, etc.)
    • weight per ml.(e.g. for solutions, injections, etc.)
    • quantity (percentage or amount) per measured dose(e.g. oral liquids, metered aerosols, drops, etc.)
  • Metric weights and measures shall be used.
  • In cases where product contains active ingredient(s) that cannot be definitely identified state the name of the material to which activity is ascribed and, where appropriate, the potency or activity of the product.

Remarks on active  ingredient (if any): 

  • This field shall be used where the raw material in product formulation yields an equivalent active component.After each ingredient entry is correctly made, click the ‘add/ save’ button. The remove button will allow for corrections to an entry under this heading. To remove item, select item from the listing and click remove. 

How to Access Active Ingredient in QUEST3+ System ? 

Product Registration >> New Application Form >> Product Validation >> Active Ingredients

National Pharmaceutical Regulatory Agency (NPRA)
Lot 36, Jalan Universiti, 46200 Petaling Jaya, Selangor, Malaysia.
  • Email: npra@npra.gov.my
  • Phone: +603-7883 5400
  • Fax: +603-7956 2924, +603-7956 7075

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The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

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  • Last Modified: Thursday 25 April 2019, 15:35:47.
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