Hydrocodone Bitartrate And Acetaminophen Tablet
Product Images NDC 43386-357

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Hydrocodone Bitartrate And Acetaminophen (NDC 43386-357). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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

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Chemical structure of Hydrocodone Bitartrate and Acetaminophen, including molecular formulas and molecular weight (M.W. 494.49). The illustration shows the detailed structural formula of the active ingredients in the drug.*

FDA Label Image

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Chemical structure diagram showing a benzene ring with a hydroxyl group (OH) and an acetamide group (NHCOCH3), identified as part of the active ingredient hydrocodone bitartrate and acetaminophen. The molecular formula C8H9NO2 and molecular weight 151.16 are displayed.*

FDA Label Image

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Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 5 mg/325 mg, oral tablets. The label indicates a package of 100 tablets by Lupin Pharmaceuticals, Inc. It includes dosage strength, pharmacist dispensing instructions, storage conditions, manufacturer details, and a barcode. The label also notes prescription status (Rx only).*

FDA Label Image

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Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5 mg/325 mg oral tablets by Lupin Pharmaceuticals, Inc. The label states Rx only, contains 30 tablets, and provides usage directions, storage instructions, and manufacturer information. The NDC number 43386-357-03 is shown with a barcode.*

FDA Label Image

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Label for Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/325 mg strength, oral tablets. The label indicates 100 tablets per package, manufactured for Lupin Pharmaceuticals, Inc. It includes storage instructions, pharmacist dispensing guide, and dosage information. The label also displays the NDC 43386-358-01 and bar code.*

* 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.