Guest
Guest
Nov 27, 2025
11:10 PM
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Under the law in India (the Drugs and Cosmetics Rules, 1945), the manufacturer (or the “marketing?authorisation holder” for that product) is responsible for ensuring the medicine is correctly labelled before it is sold.
Malegra DXT Plus means the company that manufactures or imports the drug must put necessary details on the label — including the name of the drug, active ingredients, strength, manufacturing licence number, batch number, manufacturing and expiry dates, storage instructions, and any required warnings.
Additionally, as per recent regulatory clarifications, if a “marketer” sells or distributes a drug (even if not the original manufacturer) under their branding or labelling, the marketer also shares legal responsibility for regulatory compliance — including correct labeling.
Finally, overall standards and rules for what must appear on drug labels are overseen by the national regulator Central Drugs Standard Control Organisation?(CDSCO), which enforces compliance with the Drugs and Cosmetics Act.
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