Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 67296-2305

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 67296-2305). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Metformin-fig-1.jpg (Metformin Fig 1)

Metformin-fig-1.jpg (Metformin Fig 1)
The label for Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, shows a blister pack containing 30 tablets. It displays the drug name prominently in bold with strength highlighted in gold. The label includes storage instructions, manufacturer details (Laurus Generics Inc. and Laurus Labs Limited), and a barcode on the right side. The label verifies it is prescription-only medication and shows the NDC 42385-977-30.*
FDA Label Image

Metformin-fig-2.jpg (Metformin Fig 2)

Metformin-fig-2.jpg (Metformin Fig 2)
A blister card label containing multiple individual labels for Metformin Hydrochloride Extended-Release Tablets, USP, each showing a strength of 500 mg. The labels indicate prescription-only status, manufacturing by Laurus Labs Limited, and include a barcode, lot, and expiration date fields. The product is presented as an oral extended-release tablet.*
FDA Label Image

Metformin-fig-3.jpg (Metformin Fig 3)

Metformin-fig-3.jpg (Metformin Fig 3)
Metformin Hydrochloride Extended-Release Tablets, USP 500 mg carton for institutional use only. Contains 150 (15 x 10) Unit-Dose Tablets. Manufactured for Laurus Generics Inc. and by Laurus Labs Limited, India. Includes storage instructions and a barcode. Label features the Laurus Labs logo.*
FDA Label Image

Metformin-fig-4.jpg (Metformin Fig 4)

Metformin-fig-4.jpg (Metformin Fig 4)
Label for Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg strength. The label indicates a count of 30 tablets and includes storage instructions, manufacturer details (Laurus Generics Inc. and Laurus Labs Limited), a barcode, and a note that the product is prescription only. The label emphasizes not using if the inner seal is broken and dispensing in a light-resistant container.*
FDA Label Image

Metformin-fig-5.jpg (Metformin Fig 5)

Metformin-fig-5.jpg (Metformin Fig 5)
Label sheet showing multiple identical labels for Metformin Hydrochloride Extended-Release Tablet, USP 750 mg. Each label includes a barcode, NDC 42385-978-17, manufacturer Laurus Labs Limited, and placeholders for lot and expiration dates. The labels specify prescription-only status and display the product name and strength prominently.*
FDA Label Image

Metformin-fig-6.jpg (Metformin Fig 6)

Metformin-fig-6.jpg (Metformin Fig 6)
Packaging label for Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg. The label indicates 150 unit-dose tablets (15 x 10) for institutional use only and is labeled Rx only. Manufactured by Laurus Labs Limited and for Laurus Generics Inc. The label includes storage instructions and a barcode.*

* 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.