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Labetalol batch recalled due to wrong dosage labelling

The Pharmacist

A batch of Labetalol 200mg tablets has been recalled as they are incorrectly labelled as 100mg tablets on the foil blister packaging. But the Medicines Healthcare Products Regulatory Agency (MHRA) said that the actual tablets were 200g strength, consistent with the information on the outside of the box.

Dosage 98
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Sustainable pharma packaging: breaking down the barriers to adoption

European Pharmaceutical Review

For most consumers, product packaging represents their first impression of a brand and its sustainability credentials. But how is this push shaping the pharma packaging market and what are the key changes we can expect to see? For many, aesthetic appeal and user experience top the list of priorities when it comes to packaging design.

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Labelling of Dispensed Medicine

RX Note

Present complex information in lists rather than paragraphs when possible. Use numbers rather words to convey numeric information, for example 'take 2 tablets.' capitals, bolding and highlighting) to communicate important information. drug dosage) and the indications of medication (e.g. 12 point and above).

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The Benefits of Blister Packaging

Pharma Packaging Solutions

If you have ever taken any kind of medication, be it prescription or over the counter (and you almost certainly have), then you’re probably familiar with blister packaging. Blister packaging is extremely common in the pharmaceutical industry, thanks to its many benefits. Intuitive Dosage. Convenience. Regulate Routine.

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We, at OmniActive, invest over 10 per cent of the total outlay into R&D

Express Pharma

This enables us to optimise dosages in our final products, enhancing both bioavailability and patient safety. By providing clear information about our bioactives, we aim to boost consumer confidence, ultimately driving sales and improving profitability. This transparency reinforces their decision to prioritise quality over cost.

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Navigating the Generic Drug Approval Process: A Comprehensive Guide

Drug Patent Watch

Step 2: ANDA Filing Generic drug manufacturers submit an Abbreviated New Drug Application (ANDA) to the FDA, which includes detailed information about the proposed generic drug, including its active ingredients, dosage forms, and manufacturing processes. This includes providing clear instructions for use, warnings, and precautions.

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Educating Patients about Generic Drugs: Strategies for Success

Drug Patent Watch

As healthcare professionals, it’s our responsibility to educate patients about generic drugs and empower them to make informed decisions about their treatment options. Mobile Apps Develop or recommend mobile apps that provide information about generic drugs, compare prices, and offer medication reminders.