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Glipizide And Metformin Hydrochloride Tablet, Film Coated
Product Images NDC 0093-7455
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Glipizide And Metformin Hydrochloride (NDC 0093-7455). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Teva Pharmaceuticals Usa, 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.
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This is a pharmaceutical product called Metformin Hydrochloride Tablets with a strength of 2.5 mg/250 mg. The tablets come in a bottle with 100 pieces and have a film coating. The product is for prescription only and includes warnings to keep it out of reach of children. The product appears to be manufactured in Israel by Teva Pharmaceuticals and distributed in the USA by Teva Pharmaceuticals USA, Inc. There are dosage instructions in the package insert. There is a serialization coding area on the packaging.*
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This is a description of a medication called Metformin Hydrochloride Tablets, USP, with a strength of 2.5 mg/500 mg. The medication comes in a bottle with 100 coated tablets and has an NDC number of 0093-7456-01 and a GTIN number of 00300937456018. The accompanying patient information leaflet should be dispensed with the medication by the pharmacist. The medication should be stored at 20° to [see USP Cor]. The package insert should be referred to for complete prescribing information. The medication should be kept out of the reach of children. The medication is manufactured by Teva Pharmaceuticals in Kfar Saba, 44102 and is manufactured for Teva Pharmaceuticals USA in Parsippany, NJ 07054. The code "323K32686-02" is present in the Serialization Coding Area.*
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This is a description of Metformin Hydrochloride Tablets, USP with a strength of 5mg/500mg. It is intended for dispensing by a pharmacist and comes with 100 tablets and an accompanying patient information leaflet. The tablets are film-coated and are manufactured by Teva Pharmaceutical Industries in Kfar Saba, Israel for distribution by Teva Pharmaceuticals USA in Parsippany, NJ. The product's NDC code is 0093-7457-01 and its GTIN is 00300937457015. The product should be kept out of reach of children. The provided text also includes a manufacturing date and a serialization coding area.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
