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             Are Generic drugs safe?:: Canadian pharmacies online

  The common question is whether generic drugs are safe or no? You know a generic drug is the same as a brand-name in safety, dosage, strength, quality and their performance, and intended use.

  Generic drugs are approved by FDA (Food and Drug Administration). The FDA requires that generic drugs have the same quality, strength, purity and stability as brand-name drugs. A generic drug must contain the same amount of active ingredient. A Canadian pharmacies that wishes to market their generic drug must offer proof of bioequivalence and bioavailability to the FDA. The production, packaging, and distribution of generic drugs is tightly regulated by the Food and Drug Administration and generic drugs are subject to the same strict rules of purity, strength, and quality as brand name drugs as laid down by respective pharmacopoeia.

  So we truly believe that generic drugs are as safe and effective as the brand name. Generic drugs are the same in dosage, strength, safety, efficacy, and intended use to the brand name drugs even if they have a different color or shape than the brand name drug. The FDA requires all drugs, including brand name drugs and generic drugs must work well and be safe.

FDA requirements for generic drugs: Canadian pharmacies online

1-The Generic Drug must have the same active ingredient and the same labeled strength as the brand-name product.

2-It must have the same dosage form-tablets, capsules, ointments, patches or liquids are examples of dosage forms

3-The generic drug's labeling must be essentially the same as that of the approved drug.

4-The firm must fully document the Generic Drug's chemistry, manufacturing steps, and quality control measures. Each step of the process are detailed for FDA before approal.

5-Firms must assure the FDA that the raw materials and finished product meet specifications of the U.S. Pharmacopoeia, the organization that sets standards for drug purity in the United States.

6-Generic Drugs must be bioequivalent and therapeutically equivalent to their brand-name

7-Firms must show that a generic drug will maintains stability under extremes of heat and humidity until the expiration date on the label

8-Before FDA approves a generic drug, it must be conducts an inspection at the proposed manufacturing site to make sure the firm is capable of meeting its application commitments and to ensure the firm can manufacture the product consistently.