Butalbital, Acetaminophen And Caffeine Tablet
Product Images NDC 70010-149

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Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Butalbital, Acetaminophen And Caffeine (NDC 70010-149). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules Pharmaceuticals Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

100-labe (100 Label)

100-labe (100 Label)
NDC 70010-149-01 is the identification code for Butalbital, Acetaminophen, and Caffeine Tablets, USP. Each tablet contains 50 mg of Butalbital, 325 mg of Acetaminophen, and 40 mg of Caffeine. It is a prescription drug that comes in a container with 100 tablets. The recommended dose should not exceed four tablets in a day, with an interval of 4 hours between each dose. It's advised to keep the drug out of reach of children and store it in a tight, light-resistant container at a temperature between 20°C to 25°C. This medication is made by Grinuies Pharmaceutical, Inc., in Cranbury, VA.*
FDA Label Image

500-labe (500 Label)

500-labe (500 Label)
The NDC 70010-149-05 C medicine contains Butalbital, Acetaminophen, and Caffeine tablets, with the quantity of 50mg/325mg/40mg, and it is available under prescription only. The recommended adult dosage is 1 or 2 tablets every four hours but should not exceed 6 tablets in a day. The medicine should be stored between 20°C to 25°C, and it should be kept in a tight, light-resistant container as defined in the USP. The manufacturer of this medicine is Granules Pharmaceuticals, Inc., situated at Chantilly, VA 20151.*
FDA Label Image

Fig-1 (Figure 1)

FDA Label Image

Fig-2 (Figure 2)

FDA Label Image

Fig-3 (Figure 3)

* 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.