Omeprazole Capsule, Delayed Release
Product Images NDC 70518-0199

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 Omeprazole (NDC 70518-0199). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Omeprazole 40mg 70518 0199 00

Omeprazole 40mg 70518 0199 00
Omeprazole 40 mg delayed-release capsules label showing the product name, strength, dosage form, and quantity of 90 capsules. The label includes the REMEDYREPACK INC. logo and states that the product is prescription only (Rx only). Manufacturer is Glenmark, Mahwah, NJ, with a barcode and QR code visible. Additional instructions advise seeing the package insert for directions and note storage conditions.*
FDA Label Image

Mm2 (Omeprazole 40mg 70518 0199 01)

Mm2 (Omeprazole 40mg 70518 0199 01)
Label for Omeprazole 40 mg delayed-release capsules, with a quantity of 30. The label includes the NDC 70518-0199-01 and states the product is RX only. It is repackaged by RemedyRepack Inc. and originally manufactured by Glenmark, Mahwah, NJ. Storage instructions and a barcode are also visible.*
FDA Label Image

Omeprazole 40mg 70518 0199 02

Omeprazole 40mg 70518 0199 02
Label for Omeprazole 40 mg delayed-release capsules, quantity 30, repackaged by RemedyRepack Inc. The label includes the NDC number 70518-0199-02 and notes the manufacturer as Glenmark, Mahwah, NJ. It provides storage instructions and a QR code along with a barcode on a white background with purple accents.*

* 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.