Alprazolam
Product Images NDC 67296-1748

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Alprazolam (NDC 67296-1748). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Label (67296 1748)

Alprazolam 0.25 mg label with quantity of 10 tablets. The label shows the NDC 67296-1748-1, Rx only designation, lot number 190840X1, and expiration date 04/21. It includes storage instructions to keep at controlled room temperature (20-25°C/68-77°F). The manufacturer is Centaur Pharmaceuticals Pvt Ltd, Maharashtra, India, and the distributor is Redpharm Drug, Eden Prairie, MN.*

FDA Label Image

Chemical Structure (Alprazolam 01)

Chemical structure diagram of the active ingredient Alprazolam, showing its fused benzodiazepine ring system with chlorine and phenyl substituents as represented in the image.*

FDA Label Image

Image (Alprazolam 02)

The image shows a blister package containing four white, oval-shaped tablets arranged in a single row. The tablets are uncoated and have a scored line down the middle, dividing each into two halves. There is no visible text or logo on the tablets or the packaging in the image.*

FDA Label Image

Image (Alprazolam 03)

Packaging label for Alprazolam tablets from RedPharm Drug, Inc. The image shows a white elongated oval tablet with two score lines on one side, dividing the tablet into three sections with debossed markings.*

FDA Label Image

Image (Alprazolam 04)

Chemical structure diagram showing the molecular arrangement of Alprazolam, the active ingredient in the product labeled by RedPharm Drug, Inc. The diagram illustrates the bonds and atom connectivity typical of this benzodiazepine compound.*

FDA Label Image

Principal Display Panel (0.25 mg Tablet Bottle Label)

Label for Alprazolam Tablets, USP 0.25 mg. The label includes barcode and QR code information, dosage strength, manufacturer Centaur Pharmaceuticals Pvt. Ltd. India, and distributor Breckenridge Pharmaceutical, Inc. USA. It notes storage instructions, packaging quantity of 100 tablets, and directions for the pharmacist to dispense medication guide with each patient.*

FDA Label Image

Principal Display Panel (0.5 mg Tablet Bottle Label)

Alprazolam Tablets USP 0.5 mg label showing product name, strength, dosage form, and packaging details. The label includes manufacturer Centaur Pharmaceuticals Pvt. Ltd. and distributor Breckenridge Pharmaceutical, Inc. The label notes storage instructions and dosage use information for 100 tablets.*

FDA Label Image

Principal Display Panel (1 mg Tablet Bottle Label)

Alprazolam Tablets, USP 1 mg label from RedPharm Drug, Inc. The label includes the NDC 51991-706-01, dosage strength 1 mg, and storage instructions to keep at 20° to 25°C (68° to 77°F). It notes the tablets should be dispensed in tight, light-resistant containers and includes manufacturer information from Centaur Pharmaceuticals Pvt. Ltd. and distributor details for Breckenridge Pharmaceutical, Inc. The package contains 100 tablets.*

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Alprazolam Tablets, USP 2 mg, in a rectangular label format showing dosage strength prominently. The label includes barcodes, the NDC number 51991-707-01, dispensing instructions, storage conditions, and manufacturer details indicating CENTAUR PHARMACEUTICALS PVT. LTD. The label also mentions that it contains 100 tablets, is for Rx only, and includes lot and expiration placeholders.*

* 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.