Isotretinoin Capsule
Product Images NDC 70710-1022

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Isotretinoin (NDC 70710-1022). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals Usa 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 Isotretinoin, showing its molecular framework including rings and conjugated double bonds, with a carboxyl group (COOH) at one end.*

FDA Label Image

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Packaging label for Isotretinoin Capsules USP 10 mg by Zydus Pharmaceuticals USA Inc. The carton includes storage instructions, warnings against use during pregnancy, and dispensing information. It contains 3 prescription blister packs with 10 capsules each, for oral administration. The label highlights the active ingredient strength and includes barcode and regulatory information.*

FDA Label Image

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Packaging label artwork for Isotretinoin capsules by Zydus Pharmaceuticals USA Inc. The label is for prescription oral capsules, displaying reminders for pharmacists about dispensing restrictions and patient communication, as well as special instructions for pharmacists regarding the IPLEDGE program. The design is a flat fold-out carton template with text boxes containing these instructions.*

FDA Label Image

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Packaging label for Isotretinoin Capsules, USP 20 mg in an oral capsule dosage form by Zydus Pharmaceuticals USA Inc. The label indicates this is a prescription drug with directions for pharmacists and warnings about use in pregnancy. The box contains 3 prescription blister packs, each with 10 capsules (30 capsules total). The label includes storage instructions and patient safety warnings.*

FDA Label Image

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This image shows a flat die-cut packaging label intended for an isotretinoin capsule carton by Zydus Pharmaceuticals USA Inc. The label includes text sections with reminders for pharmacists about dispensing instructions, authorization, and patient information. There is no visible branding, dosage strength, or capsule imagery on the label in this flattened layout.*

FDA Label Image

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Label for Isotretinoin Capsules USP 30 mg oral capsules by Zydus Pharmaceuticals USA Inc. The packaging includes instructions, warnings, and details on prescription dispensing. It states the product is for oral use, contains 3 prescription blister packs with 10 capsules each, and includes specific storage information. The design emphasizes child-resistant packaging and safety warnings about pregnancy and proper use.*

FDA Label Image

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Packaging label template for Isotretinoin capsules by Zydus Pharmaceuticals USA Inc., showing unfolded carton layout including sections for patient and pharmacist instructions. Text areas mention dispensing restrictions and medication guides but strength and count details are not visible on this image.*

FDA Label Image

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Isotretinoin Capsules, USP 40 mg oral capsules carton labeled by Zydus Pharmaceuticals USA Inc. The carton includes a clear display of the proprietary and generic name, strength of 40 mg, and instructions for pharmacist and patient. Warnings include contraindication in pregnancy, with specific handling and storage instructions. The packaging also indicates prescription status and contains multiple blister packs of capsules.*

FDA Label Image

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Flat packaging label layout for Isotretinoin capsules by Zydus Pharmaceuticals USA Inc. The label includes sections for pharmacy reminders and special instructions for pharmacists. The design is for a multi-dose carton, likely accommodating capsules in multiple strengths but no specific strength or count is visible in the image.*

* 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.