Metformin Hydrochloride Tablet
Product Images NDC 50228-105

10 FDA label images from Sciegen Pharmaceuticals Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 50228-105). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sciegen 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

Metformin 105 01

Metformin 105 01
Label of Metformin Hydrochloride Tablets, USP 500 mg by ScieGen Pharmaceuticals Inc. The label includes storage instructions, usual dosage note, and indicates the package contains 100 tablets for oral use. It features a barcode and the NDC number 50228-105-01.*
FDA Label Image

Metformin 105 05

Metformin 105 05
Metformin Hydrochloride Tablets, USP 500 mg oral tablets label showing a count of 500 tablets. The label includes storage instructions, manufacturer ScieGen Pharmaceuticals Inc, and a barcode. The packaging specifies prescription use only and mentions dispensing in a light-resistant container.*
FDA Label Image

Metformin 105 10

Metformin 105 10
Label for Metformin Hydrochloride Tablets, USP 500 mg oral tablets, containing 1,000 tablets per container. The label includes storage instructions, dosage caution, and manufacturer details for ScieGen Pharmaceuticals Inc., Hauppauge, NY. It features a barcode and indicates Rx only.*
FDA Label Image

Metformin 106 01

Metformin 106 01
Label for Metformin Hydrochloride Tablets, USP, 850 mg, oral tablets. The package contains 100 tablets and is labeled Rx Only. The label includes storage instructions, dosage directions, and the manufacturer ScieGen Pharmaceuticals, Inc. A barcode is present along with the NDC 50228-106-01.*
FDA Label Image

Metformin 106 05

Metformin 106 05
Label for Metformin Hydrochloride Tablets, USP, 850 mg oral tablets. The label indicates a package of 500 tablets, Rx only. It includes storage instructions and mentions ScieGen Pharmaceuticals Inc as the manufacturer, located in Hauppauge, NY. A barcode and NDC 50228-106-05 are also visible.*
FDA Label Image

Metformin 106 10

Metformin 106 10
Label for Metformin Hydrochloride Tablets USP 850 mg in a 1,000 tablet count bottle by ScieGen Pharmaceuticals Inc. The label includes storage instructions, prescribing information note, and the NDC 50228-106-10. It also features a barcode and the note 'NO VARNISH'.*
FDA Label Image

Metformin 107 01

Metformin 107 01
Label for Metformin Hydrochloride Tablets, USP 1000 mg by ScieGen Pharmaceuticals Inc. The label includes dosage form (tablets), package size (100 tablets), NDC number, storage instructions, and indication that the product is prescription-only (Rx Only). The label states "NO VARNISH" on the right edge and includes the ScieGen logo.*
FDA Label Image

Metformin 107 05

Metformin 107 05
Label for Metformin Hydrochloride Tablets, USP, 1000 mg oral tablets by ScieGen Pharmaceuticals Inc. The label states the package contains 500 tablets with Rx only. It includes instructions to read prescribing information and storage conditions, barcode, and manufacturer details.*
FDA Label Image

Metformin 107 10

Metformin 107 10
Label for Metformin Hydrochloride Tablets, USP 1000 mg oral tablets, packaged as 1,000 tablets. The label includes storage instructions and manufacturer information for ScieGen Pharmaceuticals Inc. The NDC code is 50228-107-10.*
FDA Label Image

Met Structure

Met Structure
Chemical structure of metformin hydrochloride showing its molecular arrangement with methyl groups, nitrogen atoms, and hydrochloride component.*

* 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.