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Pharmaceutical Regulatory Affairs: Open Access

ISSN: 2167-7689

Open Access

Bahmani K


Bhiwani, Haryana
India

Publications
  • Review Article
    Generic Drugs, A Need to the Public: USA and India- Government Plans to Reduce the Price of ANDA and List of Generic Drugs Approved in Year 2018
    Author(s): Bahmani K and Martin RBahmani K and Martin R

    Health is the prime component for every person and in the world, there are different traditions have their own approaches to treat and cure illness. The dosage form of the drug may appear different but medically, however a generic medicament has the same mechanism in the body as that of the costlier brand-name drugs. They acquire the equal active ingredient and must pass the same satisfactory standards with respect to manufacturing and packaging of medicaments. The Generic medicinal drug beneath the regulation of U.S. Food and Drug Administration must have the equal quality and performance as that of the of brand-name drugs. The FDA states: “Generics have the identical quality as brand identify drugs. When a generic drug product is approved, it has met rigorous standards established via the FDA with respect to identity, strength, quality, purity, and potency. India started Jan A.. Read More»

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Google Scholar citation report
Citations: 533

Pharmaceutical Regulatory Affairs: Open Access received 533 citations as per Google Scholar report

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