Chlorpromazine Hydrochloride Tablet, Film Coated
Product Images NDC 70710-1133

11 FDA label images from Zydus Pharmaceuticals (usa) Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Chlorpromazine Hydrochloride (NDC 70710-1133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus 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.

FDA Label Image

Image (B9b68d15 Cd69 4896 A02e A09c6f07ce82 01)

Image (B9b68d15 Cd69 4896 A02e A09c6f07ce82 01)
Chemical structure diagram of Chlorpromazine hydrochloride, showing its molecular formula C17H19ClN2S with hydrochloride and molecular weight 355.33.*
FDA Label Image

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 02)

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 02)
Chlorpromazine Hydrochloride Tablets, USP 10 mg film-coated oral tablets, labeled for 100 tablets per package. The NDC number 70710-1129-1 is visible. Manufactured by Zydus Lifesciences Ltd., India, and distributed by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ. The label includes storage instructions and a child-resistant packaging warning.*
FDA Label Image

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 03)

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 03)
Packaging label for Chlorpromazine Hydrochloride Tablets, USP 10 mg film-coated tablets by Zydus Pharmaceuticals (USA) Inc. The label indicates a package size of 100 tablets (10 x 10 unit-dose), includes storage instructions, a barcode, and manufacturer information showing distribution by Zydus Pharmaceuticals (USA) Inc. The label notes the unit dose package is not child-resistant.*
FDA Label Image

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 04)

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 04)
Label for Chlorpromazine Hydrochloride Tablets, USP 25 mg, film-coated oral tablets. The label indicates a package of 100 tablets, prescription only, manufactured by Zydus Lifesciences Ltd. and distributed by Zydus Pharmaceuticals (USA) Inc. It includes storage instructions, emphasizes child resistance, and displays the NDC 70710-1130-1 with the Zydus logo.*
FDA Label Image

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 05)

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 05)
Packaging label for Chlorpromazine Hydrochloride Tablets, USP 25 mg, film-coated oral tablets. The label states the product contains 100 tablets (10 x 10 unit-dose) and notes it is not child-resistant. It includes storage instructions to keep at 20° to 25°C and warnings to keep out of reach of children. The label shows the Zydus Pharmaceuticals logo and lists Zydus Pharmaceuticals (USA) Inc. as the distributor and Zydus Lifesciences Ltd. as the manufacturer.*
FDA Label Image

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 06)

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 06)
Chlorpromazine Hydrochloride Tablets, USP 50 mg film-coated oral tablets packaging label by Zydus Pharmaceuticals (USA) Inc. The label includes the NDC 70710-1131-1, states it contains 100 tablets, and notes Rx only. Manufacturer is Zydus Lifesciences Ltd., India, with distribution by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ.*
FDA Label Image

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 07)

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 07)
Packaging label for Chlorpromazine Hydrochloride Tablets, USP 50 mg film-coated tablets. The label shows the product name prominently with strength, dosage form, and a quantity of 100 tablets (10 x 10 unit-dose). It includes storage instructions, manufacturer and distributor information, NDC 70710-1131-4, and a barcode. The labeler is Zydus Pharmaceuticals (USA) Inc.*
FDA Label Image

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 08)

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 08)
Label for Chlorpromazine Hydrochloride Tablets, USP, 100 mg, film-coated oral tablets. The package contains 100 tablets, prescription only, manufactured by Zydus Lifesciences Ltd. and distributed by Zydus Pharmaceuticals (USA) Inc. The label includes storage instructions and drug usage notes as per USP standards.*
FDA Label Image

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 09)

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 09)
Packaging label for Chlorpromazine Hydrochloride Tablets USP 100 mg, film-coated oral tablets. The label shows the brand name chlorproMAZINE, strength 100 mg, and package size of 100 tablets (10 x 10 unit-doses). Manufactured by Zydus Lifesciences Ltd. and distributed by Zydus Pharmaceuticals (USA) Inc. The label includes storage instructions, a barcode, NDC 70710-1132-4, and notes that the unit dose package is not child-resistant.*
FDA Label Image

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 10)

Label (B9b68d15 Cd69 4896 A02e A09c6f07ce82 10)
The label for Chlorpromazine Hydrochloride Tablets, USP 200 mg, film-coated oral tablets. The packaging displays the NDC number 70710-1133-1 and indicates a 100 tablet count. The label includes manufacturer and distributor details: Zydus Lifesciences Ltd., India, and Zydus Pharmaceuticals (USA) Inc., respectively. It also states the product is Rx only and provides storage and safety information.*
FDA Label Image

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 11)

Carton (B9b68d15 Cd69 4896 A02e A09c6f07ce82 11)
Chlorpromazine Hydrochloride Tablets USP 200 mg film-coated tablet unit-dose package carton. The labeling states it contains 100 tablets (10 x 10 unit-dose). The product is manufactured by Zydus Lifesciences Ltd., India, and distributed by Zydus Pharmaceuticals (USA) Inc. Instructions include storage between 20° to 25°C and a warning that this unit-dose package is not child-resistant.*

* 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.