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Leading API chemical companies in contract marketing

Pharmaceutical Technology

Various factors have contributed to the need and growth of API chemical suppliers such as rising healthcare expenditure, increasing disposable incomes, growing geriatric population, increasing incidence of chronic diseases, patent expiration of blockbuster drugs, increased consumption of generic drugs, and intervention of the new generation APIs.

Marketing 130
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Leading retail pharmacies in pharma

Pharmaceutical Technology

Prescription refill and generic drug programmes. The document contains detailed information on the suppliers and their product offerings, alongside contact details to aid your purchasing or hiring decision. . ยท Compounding services. Pharmacogenetics testing. Filling services. Prescription collection lockers.

Pharmacy 147
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In the News: October Regulatory and Development Updates

Camargo

Presumably, Antaresโ€™ long-established 90-person urology sales force can achieve pull-thru of this drug product. Labeling regulations prohibit reminder ads for products with boxed warnings, which the FDA requires when a drug product has very serious risks.

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Amphastar Announces Approval for Glucagon for Injection Kit, 1mg

The Pharma Data

This further highlights Amphastarโ€™s considerable abilities to bring complex generic drugs to the market, and more specifically, our strong peptide capabilities.” sales for Eli Lillyโ€™s Glucagon Emergency Kit for Low Blood Sugar, 1 mg, were approximately $144 million, and the overall U.S. ” According to IQVIA, the U.S.

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Buscopan vs Mebeverine | OTC IBS treatment

Druggist

Mebeverine, on the other hand, is a generic name of the drug, which is also known as Colofac (brand name). Both products contain the same active ingredients regardless of whether they are prescribed or purchased over the counter: Each Buscopan tablets contains 10mg of hyoscine butylbromide. Buy on Amazon Price incl.

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In the News: November Regulatory and Development Updates

Camargo

House of Representatives passed the โ€œ Fairness in Orphan Drug Exclusivity Act โ€ to require proof from biopharma companies introducing improved versions of orphan drugs that they do not expect to recoup R&D costs through US sales in 12 years. GDUFA has changed this picture, at least for complex drug products.

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Health Canadaโ€™s proposed amendments to the Food and Drug Regulations and the Medical Devices Regulations

Pharma in Brief

Rolling submissions, which are currently in use for COVID-19 drugs, would be extended to other drugs, such as those which address significant new and emerging infectious diseases in Canada, or which treat, prevent, or diagnose serious or severely debilitating diseases or conditions. Biologic Drugs.