Minoxidil 1
Minoxidil Tablet
Product Images NDC 49884-256
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Product Visual Gallery
This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Minoxidil (NDC 49884-256). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Par Health Usa, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
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This is a medication called Minoxidil in tablet form containing 0.25mg. The typical dosage usage is not provided, but the accompanying literature should be read carefully to identify correct dosage levels. Patients should store it at controlled temperatures between 20° and 25°C (68° and 77°F), and each prescription should include one patient information sheet. It is recommended to dispensing this medication in a secure container, and it is not suitable for children. The product is distributed by Par Pharmaceutical Companies, Inc. in Chestnut Ridge, NY and manufactured by Par Formulations Private Limited in India. The licensing number is TNDDDDZWZW. The excerpt also contains additional numbers which do not seem to convey specific meanings.*
Minoxidil 13
Each tablet contains 10 mg of Minoxidil, USP. This drug is distributed by Par Pharmaceutical Companies, Inc. The usual dosage and other important instructions are mentioned in the accompanying literature. The tablets are manufactured in India by Aman Formulations Private Limited. It is important to keep this drug out of reach of children and store it in a tight container at 20° to 25°C (68° to 77°F). Prescription is required for buying the tablets and the dispensing information sheet must be included with each prescription. The expiration date is not available.*
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* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
