Celecoxib Capsule
Product Images NDC 16714-734

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Celecoxib (NDC 16714-734). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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 diagram of celecoxib featuring its distinctive sulfonamide group, trifluoromethyl group attached to a pyrazole ring, and methyl-substituted phenyl ring.*

FDA Label Image

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Label for Celecoxib Capsules 50 mg, a human prescription drug by NorthStar Rx LLC. The label includes dosage instructions, storage conditions, and manufacturer details. It features a barcode, QR code area, and space for batch overprinting of GTIN, serial number, expiry, and lot. The package contains 60 capsules, manufactured by Cipla Ltd., India.*

FDA Label Image

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Packaging label for Celecoxib Capsules 100 mg, oral dosage form. The label shows the product name, strength, form, and quantity of 100 capsules. It includes pharmacist dispensing instructions, storage conditions, and manufacturer information for NorthStar Rx LLC and Cipla Ltd. The label includes the NDC code 16714-732-01 and a barcode.*

FDA Label Image

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Label for Celecoxib Capsules 200 mg by NorthStar Rx LLC. The label indicates 100 capsules in the package, for oral use only with directions for pharmacists to dispense the accompanying medication guide. Manufactured by Cipla Ltd., India, with storage instructions and regulatory information included.*

FDA Label Image

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Label for Celecoxib Capsules 400 mg oral dosage form, with 60 capsules per container. The label indicates prescription only use, manufactured for NorthStar Rx LLC and by Cipla Ltd. It includes storage instructions, a barcode, and a note about batch information being overprinted during commercial packaging.*

* 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.