Nicardipine Hydrochloride Capsule
Product Images NDC 62559-206

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nicardipine Hydrochloride (NDC 62559-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani Pharmaceuticals, 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

Structure (Image 01)

Structure (Image 01)
Chemical structure diagram of nicardipine hydrochloride, showing its molecular components and arrangement including aromatic rings, nitro group, ester, and hydrochloride salt.*
FDA Label Image

Label (20 mg)

Label (20 mg)
Label for Nicardipine Hydrochloride Capsules 20 mg by ANI Pharmaceuticals, Inc. The label states the capsules contain 20 mg of Nicardipine Hydrochloride USP and are packaged in a quantity of 90 capsules. The label includes storage instructions, child-resistant container information, and manufacturer details for ANI Pharmaceuticals Canada, Inc., Oakville, ON, and distributor ANI Pharmaceuticals, Inc., Baudette, MN.*
FDA Label Image

Label (30 mg)

Label (30 mg)
Nicardipine Hydrochloride Capsules 30 mg label showing the product name, strength, and dosage form. The label states the product is for prescription use only (Rx only) and contains 90 capsules. Manufactured by ANI Pharmaceuticals Canada, Inc. and distributed by ANI Pharmaceuticals, Inc. Location details and storage instructions (20° to 25°C) are also shown. A barcode, QR code, and lot/expiration data placeholders are visible.*
FDA Label Image

Logo (Image 04)

* 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.