Haloperidol Tablet
Product Images NDC 59651-794

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Haloperidol (NDC 59651-794). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label.principal Display Panel (0.5 mg (100 Tablets Bottle))

Package Label.principal Display Panel (0.5 mg (100 Tablets Bottle))
Label for Haloperidol Tablets, USP 0.5 mg oral tablets, containing 100 tablets per container. Manufactured by Aurobindo Pharma Limited and distributed by Aurobindo Pharma USA, Inc. The label includes dosage warnings, storage instructions, and a barcode. It shows a sample image of a round, white tablet marked with '0.5'.*
FDA Label Image

Package Label.principal Display Panel (1 mg (100 Tablets Bottle))

Package Label.principal Display Panel (1 mg (100 Tablets Bottle))
Haloperidol Tablets USP 1 mg oral tablets packaging label by Aurobindo Pharma Limited. The label shows a count of 100 tablets. Storage instructions indicate keeping the product at 20° to 25°C with permitted excursions, and protection from light. The label includes distribution information for Aurobindo Pharma USA, Inc., and shows a sample tablet image marked HL 1.*
FDA Label Image

Package Label.principal Display Panel (2 mg (100 Tablets Bottle))

Package Label.principal Display Panel (2 mg (100 Tablets Bottle))
Haloperidol Tablets USP 2 mg oral tablets packaging label from Aurobindo Pharma Limited. The label states the strength as 2 mg and package contains 100 tablets. It includes storage instructions and a representation of the round, light-colored tablet marked 'HL 2'. Distributed by Aurobindo Pharma USA, Inc., made in India.*
FDA Label Image

Package Label.principal Display Panel (5 mg (100 Tablets Bottle))

Package Label.principal Display Panel (5 mg (100 Tablets Bottle))
Haloperidol Tablets, USP 5 mg oral tablets label by Aurobindo Pharma Limited. The label shows a round, light-colored tablet imprinted with "HL" above the score line and "5" below. Packaging indicates 100 tablets with storage instructions and distributed by Aurobindo Pharma USA, Inc. Barcode and NDC number 59651-792-01 are also visible.*
FDA Label Image

Package Label.principal Display Panel (10 mg (100 Tablets Bottle))

Package Label.principal Display Panel (10 mg (100 Tablets Bottle))
Label for Haloperidol Tablets, USP 10 mg oral tablets by Aurobindo Pharma Limited, with package size of 100 tablets. The label includes storage instructions, dosing note, manufacturer information, and an image of a single round green tablet imprinted with HL and 10.*
FDA Label Image

Package Label.principal Display Panel (20 mg (100 Tablets Bottle))

Package Label.principal Display Panel (20 mg (100 Tablets Bottle))
Label for Haloperidol Tablets, USP 20 mg, a prescription oral tablet by Aurobindo Pharma Limited. The label shows a blue tablet engraved with 'HL 20' and indicates packaging of 100 tablets. It includes storage instructions, distributor information (Aurobindo Pharma USA, Inc.), and a barcode. The label emphasizes keeping the medication out of children's reach and protecting it from light.*
FDA Label Image

Str (Haloperidol Str)

Str (Haloperidol Str)
Chemical structure of Haloperidol, showing its molecular formula C21H23ClFNO2 and molecular weight 375.87. The structure includes aromatic rings with chlorine and fluorine substituents, and functional groups typical of Haloperidol.*

* 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.