Pantoprazole Sodium Delayed-release Tablet
Product Images NDC 70756-019

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 Pantoprazole Sodium Delayed-release (NDC 70756-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma 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.

FDA Label Image

1 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 01)

1 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 01)
Chemical structure of pantoprazole sodium, the active ingredient in pantoprazole sodium delayed-release tablets. The diagram shows the molecular structure including functional groups and the sodium ion complex.*
FDA Label Image

40-90 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 02)

40-90 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 02)
Label for Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg strength, oral tablets. The label includes directions to swallow whole, packaging size of 90 tablets, and manufacturer Lifestar Pharma LLC with address in Mahwah, NJ. It indicates the product is made in India and provides storage and dispensing instructions along with a QR code for the Medication Guide.*
FDA Label Image

40-1000 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 03)

40-1000 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 03)
Pantoprazole sodium delayed-release tablets, USP 40 mg, oral dosage form, 1000 tablets per container, labeled for Lifestar Pharma LLC. The label includes instructions to swallow tablets whole, storage conditions, and a QR code linking to the Medication Guide. Manufactured for Lifestar Pharma LLC in Mahwah, NJ, USA, with tablets made in India.*

* 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.