Nicardipine Hydrochloride Capsule
Product Images NDC 87564-028

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nicardipine Hydrochloride (NDC 87564-028). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amerisyn Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Image (3457f1c2 5ac9 4775 B6dd 65329593be68 01)

Image (3457f1c2 5ac9 4775 B6dd 65329593be68 01)
Chemical structure of nicardipine hydrochloride, illustrating the molecular arrangement including its characteristic rings, nitro group, ester groups, and the hydrochloride (HCl) salt component, along with a note indicating the presence of an enantiomer.*
FDA Label Image

20 mg (3457f1c2 5ac9 4775 B6dd 65329593be68 02)

20 mg (3457f1c2 5ac9 4775 B6dd 65329593be68 02)
Label for NICARDIPINE HYDROCHLORIDE Capsules 20 mg oral capsules. The label shows 90 capsules per container. It is manufactured by Aavis Pharmaceuticals and labeled for Amerisyn LLC. The label includes dosage strength, storage instructions, drug name, barcode, and child-resistant packaging notice.*
FDA Label Image

30 mg (3457f1c2 5ac9 4775 B6dd 65329593be68 03)

30 mg (3457f1c2 5ac9 4775 B6dd 65329593be68 03)
Label for NICARDIPINE HYDROCHLORIDE Capsules 30 mg by Amerisyn LLC. The label includes the NDC number 87564-028-90, indicates the product is Rx only and contains 90 capsules. Storage and dispensing instructions are also provided along with a barcode and manufacturer information for Aavis Pharmaceuticals and Amerisyn LLC.*

* 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.