Zolpidem Tablet
Product Images NDC 71093-155

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 Zolpidem (NDC 71093-155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aci Healthcare 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.

FDA Label Image

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FDA Label Image

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The text provides instructions for use of Zolpidem Tartrate G Tablets with usual adult dose and storage conditions. The tablets need to be stored in a tightly controlled room temperature protected container. The manufacturing and distribution details are also provided along with the prescribing information.*
FDA Label Image

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This is a prescription drug with the name "9055 1E601LL IV". The usual adult dose is one or two tablets at bedtime as directed. The complete prescribing information should be followed. The drug needs to be stored at a controlled room temperature of 20°- 25°C (68° - 77°F) and dispensed in a tight, light-resistant, child-resistant container. The manufacturer is The ACME Laboratories Ltd., Dhulivita, Dhamrai, Dhaka, 1350, Bangladesh, and it is distributed by ACI Healthcare USA, Inc., 10100 W. Sample Road, Suite 406, Coral Springs, FL 33065. The other information on the label includes NDC 71093-155-06 Ronly, P4 R ETRE G C, and manufacturing/expiry dates.*
FDA Label Image

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FDA Label Image

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This is a medication label information for Zolpidem Tartrate Tablets, which should be taken as directed by a physician, typically one or two tablets at bedtime. The medication should be stored in a controlled room temperature and dispensed in a tight, light-resistant child-resistant container. The medication is manufactured by ACME Laboratories Ltd. in Bangladesh and distributed by ACI Healthcare USA, Inc. in Florida. The label includes the NDC number, prescription expiration date, and lot number. The pharmacist is advised to dispense the tablets with a medication guide. No other relevant information is available.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.