Minocycline Hydrochloride Capsule
Product Images NDC 13668-484

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Minocycline Hydrochloride (NDC 13668-484). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Torrent Pharmaceuticals Limited, 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 Minocycline Hydrochloride showing its molecular formula C23H27N3O7•HCl and molecular weight 493.95. The diagram includes functional groups such as hydroxyl (OH), amide (CONH2), and dimethylamine (N(CH3)2) moieties.*

FDA Label Image

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FDA Label Image

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Label for Minocycline Hydrochloride Capsules, USP 50 mg oral capsules. The package contains 100 capsules. The label includes storage instructions, pharmacy dispensing information, manufacturer Torrent Pharmaceuticals Limited, and an NDC number 13668-482-01. The label indicates prescription use only.*

FDA Label Image

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Label for Minocycline Hydrochloride Capsules, USP 50 mg, oral capsule dosage form, supplied in a package of 100 capsules. This prescription drug label includes storage instructions and manufacturer information, showing the labeler as Torrent Pharmaceuticals Limited. The label states the product is Rx only and notes to dispense the accompanying patient information sheet.*

FDA Label Image

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Minocycline Hydrochloride Capsules, USP 50 mg oral capsules in a bottle label format. The label states 100 capsules per container, manufactured by Torrent Pharmaceuticals Limited. It includes dosage, storage instructions, and a barcode. The label cautions Rx only and instructs pharmacists to dispense the patient information sheet.*

FDA Label Image

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Label for Minocycline Hydrochloride Capsules, USP 75 mg, oral dosage form. The label indicates the product contains 100 capsules and is for prescription use only. It includes storage instructions, a barcode, and is manufactured by Torrent Pharmaceuticals Limited.*

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Label for Minocycline Hydrochloride Capsules, USP 75 mg, containing 100 capsules. The label includes storage instructions and dosage details, with the product manufactured by Torrent Pharmaceuticals Limited. It features a barcode and the statement 'Rx only.'*

FDA Label Image

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Minocycline Hydrochloride Capsules, USP 100 mg, oral capsules, carton label for 500 capsules. The label states the product is prescription-only and instructs pharmacists to dispense the patient information sheet. Manufactured by Torrent Pharmaceuticals Limited, the label includes storage instructions and a barcode.*

FDA Label Image

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Label for Minocycline Hydrochloride Capsules, USP 100 mg by Torrent Pharmaceuticals Limited. This prescription drug label indicates a package of 50 capsules. The label includes dosing information, storage instructions, barcode, NDC 13668-484-50, and pharmacist dispensing guidance.*

FDA Label Image

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Minocycline Hydrochloride Capsules, USP 100 mg oral capsules packaging label from Torrent Pharmaceuticals Limited. The label states the quantity as 500 capsules and features the NDC number 13668-484-05. It includes pharmacist dispensing instructions and storage guidelines.*

FDA Label Image

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Label for Minocycline Hydrochloride Capsules USP 100 mg by Torrent Pharmaceuticals Limited. The label indicates a package of 50 oral capsules, with instructions to keep the drug out of reach of children and storage guidelines. It includes the NDC 13668-484-50, pharmacist dispensing information, and manufacturing details for Torrent Pharmaceuticals Ltd. and Torrent Pharma Inc.*

FDA Label Image

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Label for Minocycline Hydrochloride Capsules USP, 100 mg strength, containing 500 capsules. The label includes usage and storage instructions, pharmacist dispensing information, and manufacturer details: Torrent Pharmaceuticals Ltd, India, and Torrent Pharma Inc, USA. It displays the NDC 13668-484-05 and indicates Rx only.*

* 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.