Generic Drugs

Product Details:

Salt Composition Specific active ingredients based on the drug formulation
Pacakaging (Quantity Per Box) Varies e.g. 10 strips per box or 24 bottles per box
Origin of Medicine Manufactured using standardized processes as per GMP guidelines
Drug Type Generic
Ingredients Active pharmaceutical ingredients (API) and excipients as per formulation
Physical Form Tablets capsules syrups ointments injections
Function Treatment and management of various diseases and health conditions depending on the specific drug
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Generic Drugs Product Specifications

Physical Form Tablets capsules syrups ointments injections
Suitable For Suitable for adults children and geriatrics depending on the specific drug formulation
Dosage Varies as per the specific drug and medical prescription
Pacakaging (Quantity Per Box) Varies e.g. 10 strips per box or 24 bottles per box
Ingredients Active pharmaceutical ingredients (API) and excipients as per formulation
Quantity Depends on packaging type and order size e.g. 10 tablets per strip or 100mL syrup bottles
Origin of Medicine Manufactured using standardized processes as per GMP guidelines
Storage Instructions Store in a cool dry place away from direct sunlight and moisture
Drug Type Generic
Recommended For Patients based on prescription and specific health condition requirements
Function Treatment and management of various diseases and health conditions depending on the specific drug
Salt Composition Specific active ingredients based on the drug formulation
Dosage Guidelines Follow doctors prescription or refer to the package insert for specific dosage instructions

Product Description

A generic drug generic drugs, generics is a drug defined as "a drug product that is comparable to brand/reference listed drug product in dosage form, strength, route of administration, quality and performance characteristics, and intended use". It has also been defined as a term referring to any drug marketed under its chemical name without advertising

A generic drug must contain the same active ingredients as the original formulation. According to the U.S. Food and Drug Administration (FDA), generic drugs are identical or within an acceptable bioequivalent range to the brand-name counterpart with respect to pharmacokinetic and pharmacodynamic properties. By extension, therefore, generics are considered (by the FDA) identical in dose, strength, route of administration, safety, efficacy, and intended use

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