Minocycline Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 65862-885

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Minocycline Hydrochloride (NDC 65862-885). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (45 mg (30 Tablet Bottle))

Label for Minocycline Hydrochloride Extended-Release Tablets, USP 45 mg, film-coated tablets in a package of 30 tablets. Distributed by Aurobindo Pharma USA, Inc., made in India. The label includes storage instructions, dosage form, strength, and NDC 65862-554-30, with a barcode on the right side.*

FDA Label Image

Package Label-principal Display Panel (90 Mg (30 Tablet Bottle))

Label for Minocycline Hydrochloride Extended-Release Tablets USP, 55 mg strength, film-coated tablets. The package contains 30 tablets and is labeled for prescription use only. Distributed by Aurobindo Pharma USA, Inc., made in India. Storage instructions and warnings are also included on the label.*

FDA Label Image

Package Label-principal Display Panel (135 Mg (30 Tablet Bottle))

Label for Minocycline Hydrochloride Extended-Release Tablets, USP 65 mg, film-coated. The label indicates 30 tablets per container, distributed by Aurobindo Pharma USA, Inc., made in India. Storage instructions, barcode, and cautions about keeping out of children’s reach and dispensing in light-resistant containers are also included.*

FDA Label Image

Minocycline Fig4

Label for Minocycline Hydrochloride Extended-Release Tablets, USP 80 mg, film coated, with 30 tablets per container. Distributed by Aurobindo Pharma USA, Inc., made in India. Includes storage instructions and usage warnings with a barcode on the right side. The label features the Aurobindo logo and NDC 65862-884-30.*

FDA Label Image

Minocycline Fig5

Label for Minocycline Hydrochloride Extended-Release Tablets, USP 90 mg, film-coated, distributed by Aurobindo Pharma USA, Inc. The label indicates the product contains 30 tablets, is Rx only, and provides storage and dispensing instructions. The label includes a barcode, NDC 65862-556-30, and manufacturing details (Made in India).*

FDA Label Image

Minocycline Fig6

Minocycline Hydrochloride Extended-Release Tablets USP 105 mg label from Aurobindo Pharma. The label indicates 30 tablets per package, with directions to store at controlled room temperature and warnings to keep out of reach of children. It is distributed by Aurobindo Pharma USA, Inc., made in India. The label includes an NDC number (65862-885-30) and a barcode.*

FDA Label Image

Minocycline Fig7

Label for Minocycline Hydrochloride Extended-Release Tablets USP, 115 mg, film coated. The label states it contains 30 tablets, distributed by Aurobindo Pharma USA, Inc., with storage instructions and a barcode on the right. The label also includes the NDC 65862-557-30 and manufacturer Aurobindo Pharma Limited.*

FDA Label Image

Minocycline Fig8

Label for Minocycline Hydrochloride Extended-Release Tablets, USP 135 mg by Aurobindo Pharma Limited. The label indicates the product is prescription only and contains 30 film-coated extended-release tablets. It provides storage instructions and distributor information for Aurobindo Pharma USA, Inc., with mention of manufacturing in India and specific handling precautions.*

FDA Label Image

Chemical Structure (Minocycline Str)

Chemical structure of Minocycline Hydrochloride depicted with atomic groups and bonds, including the molecular formula C23H27N3O7·HCl and molecular weight 493.95 displayed below the structure.*

* 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.