Vancomycin Hydrochloride
Product Images NDC 76333-264

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Vancomycin Hydrochloride (NDC 76333-264). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Orient Pharma Co.,ltd Yunlin Plant, 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

Deee4d8-5254-4dd1-9a0f-d59772248a45 (Fdeee4d8 5254 4dd1 9a0f D59772248a45)

Chemical structure of vancomycin hydrochloride, depicting its complex molecular arrangement with multiple rings, hydroxyl groups, and chlorine atoms as part of the compound.*

FDA Label Image

Section16 (Section16 Table)

A table listing packaging and NDC numbers for Vancomycin capsules by Orient Pharma Co.,Ltd Yunlin Plant. It shows Vancomycin 125 mg and 250 mg strengths available in cartons containing two blister packs of 10 capsules each (20 capsules per carton) and bottles containing 50 capsules. Corresponding NDC numbers are provided for each package type and strength.*

FDA Label Image

5a12419-8079-48fc-9b85-2fae31b12ee2 (95a12419 8079 48fc 9b85 2fae31b12ee2)

Vancomycin Hydrochloride Capsule, USP 125 mg (base) label, showing a repeated sheet layout designed for individual capsule packaging. Each label includes the active ingredient and strength, NDC number 76333-264-26, Rx Only designation, manufacturer Orient Pharma Co., Ltd, Made in Taiwan, along with placeholders for bar code, lot number, and expiration date. The label also features instructions to peel to open.*

FDA Label Image

16cf3ee-89bf-41ee-8f56-0a3fa61c080c (216cf3ee 89bf 41ee 8f56 0a3fa61c080c)

Packaging label for Vancomycin Hydrochloride Capsules, USP, 125 mg equivalent. The label indicates the product contains 20 capsules (2 x 10 units-dose) and is labeled Rx only. The labeler is Orient Pharma Co., Ltd., Yunlin Plant, Taiwan. The label includes storage instructions, dosage information, and a barcode section.*

FDA Label Image

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Vancomycin Hydrochloride 250 mg (base) capsule label from Orient Pharma Co., Ltd. The label includes the product name, strength, dosage form (capsule, USP), NDC number (76333-265-26), and states it is Rx Only. It also shows manufacturer details (Orient Pharma, Co., Ltd., Made in Taiwan) and placeholders for lot number, expiration date, and bar code. The label is repeated multiple times on a sheet with peel-to-open instructions.*

FDA Label Image

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Vancomycin Hydrochloride Capsules, USP 250 mg package label from Orient Pharma Co., Ltd Yunlin Plant. The label states each capsule contains vancomycin hydrochloride equivalent to 250 mg vancomycin. The label includes storage instructions, dosage information, and manufacturer details. The package contains 20 capsules and is marked RX only.*

FDA Label Image

125bottle (125bottle)

Vancomycin Hydrochloride Capsules USP 125 mg capsule label from Orient Pharma Co., Ltd. The label states each capsule contains vancomycin hydrochloride equivalent to 125 mg vancomycin. The package contains 50 capsules. It includes storage instructions, usage warnings, and manufacturer address in Yunlin, Taiwan. The NDC number 76333-264-17 is shown along with a barcode placeholder.*

FDA Label Image

250bottle (250bottle)

Vancomycin Hydrochloride Capsules USP 250 mg label showing NDC 76333-265-17. The label states each capsule contains vancomycin hydrochloride equivalent to 250 mg vancomycin, with 50 capsules per bottle. Manufacturer is Orient Pharma Co., Ltd., Yunlin, Taiwan. Storage instructions specify controlled room temperature. The label includes dosage guidelines and a barcode area.*

* 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.