Hydralazine Hydrochloride Tablet
Product Images NDC 33342-375

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Hydralazine Hydrochloride (NDC 33342-375). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals 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

152 (Hydralazine 10 mg 1000s)

Label for Hydralazine Hydrochloride Tablets USP 10 mg, an oral prescription drug by Macleods Pharmaceuticals Limited. The label includes dosage strength, manufacturer info for Macleods Pharma USA, Inc. and Macleods Pharmaceuticals Ltd., storage instructions, and warnings to keep medication out of reach of children. Package contains 1000 tablets.*

FDA Label Image

111 (Hydralazine 10 mg 100s)

Packaging label for Hydralazine Hydrochloride Tablets, USP 10 mg, supplied as 100 tablets. The label includes the NDC 33342-374-11 and states the product is manufactured for Macleods Pharma USA, Inc. The label also provides storage instructions and dispensing guidelines. Labeler is Macleods Pharmaceuticals Limited, Baddi, Himachal Pradesh, India.*

FDA Label Image

138 (Hydralazine 10 mg 10x10s)

Hydralazine Hydrochloride Tablets, USP 10 mg oral tablets packaging label from Macleods Pharmaceuticals Limited. The label indicates a bottle containing 100 tablets (10 x 10 unit-dose). Includes manufacturer information listing Macleods Pharma USA, Inc. and Macleods Pharmaceuticals Ltd., Baddi, India. The label also notes storage instructions and that the unit-dose package is not child-resistant.*

FDA Label Image

123 (Hydralazine 100 mg 1000s)

Label for Hydralazine Hydrochloride 100 mg oral tablets, USP, manufactured by Macleods Pharmaceuticals Limited. The label indicates 1000 tablets in the package, includes storage instructions (20° to 25°C), and cautions to keep medication out of reach of children. It features a barcode and the labeler Macleods Pharma USA, Inc.*

FDA Label Image

169 (Hydralazine 100 mg 100s)

Label for Hydralazine Hydrochloride Tablets, USP 100 mg by Macleods Pharmaceuticals Limited. The label shows the product name, active ingredient strength (100 mg), and quantity (100 tablets). It includes storage instructions, manufacturer details for Macleods Pharma USA and Macleods Pharmaceuticals Ltd, and a barcode. The label is primarily white with black text and a purple box highlighting the strength.*

FDA Label Image

196 (Hydralazine 100 mg 10x10s)

Label for Hydralazine Hydrochloride Tablets, USP 100 mg, an oral tablet by Macleods Pharmaceuticals Limited. The label shows the product name and strength prominently, with packaging details indicating 100 tablets in unit-dose format. It includes manufacturer information for Macleods Pharma USA and Macleods Pharmaceuticals Ltd., along with storage instructions and a barcode.*

FDA Label Image

147 (Hydralazine 25 mg 1000s)

Label for Hydralazine Hydrochloride Tablets USP 25 mg, oral tablet form, manufactured by Macleods Pharmaceuticals Limited. The label indicates the product contains 1000 tablets and includes storage instructions, manufacturer information, and an NDC number 33342-375-44. It is intended for prescription use only.*

FDA Label Image

122 (Hydralazine 25 mg 100s)

Label of Hydralazine Hydrochloride Tablets, USP 25 mg oral tablets. The label shows the product name with strength prominently displayed, and indicates the package contains 100 tablets. It is manufactured by Macleods Pharmaceuticals Limited, with additional branding for Macleods Pharma USA. The label also includes storage instructions, prescription-only designation, and a barcode.*

FDA Label Image

157 (Hydralazine 25 mg 10x10s)

Label for Hydralazine Hydrochloride Tablets USP 25 mg by Macleods Pharmaceuticals Limited. The package contains 100 tablets in unit-dose form. The label displays the product name, strength, manufacturer details, barcode, and storage instructions. It includes a statement that the unit-dose package is not child-resistant and advises seeing the package insert for full prescribing information.*

FDA Label Image

159 (Hydralazine 50 mg 1000s)

Label for Hydralazine Hydrochloride Tablets USP 50 mg by Macleods Pharmaceuticals Limited. The label indicates the tablet strength as 50 mg, with 1000 tablets per container. It includes storage instructions and manufacturer information for Macleods Pharma USA, Inc. and Macleods Pharmaceuticals Ltd. It also references dosing and dispensing details.*

FDA Label Image

169 (Hydralazine 50 mg 100s)

Label for Hydralazine Hydrochloride Tablets, USP 50 mg oral tablets, manufactured by Macleods Pharmaceuticals Ltd. The package contains 100 tablets. The label includes dosage instructions, storage conditions (20° to 25°C), and instructions to keep the medication out of reach of children. It also lists the manufacturer location as Baddi, Himachal Pradesh, India, and distributor as Macleods Pharma USA, Inc.*

FDA Label Image

139 (Hydralazine 50 mg 10x10s)

Hydralazine Hydrochloride Tablets USP 50 mg oral tablets label. The packaging shows the brand name "hydrALAZINE" with the strength 50 mg highlighted. It is a 140-count unit-dose package (10 x 14 tablets) labeled by Macleods Pharmaceuticals Limited and Macleods Pharma USA, Inc. The label includes storage instructions and standard regulatory information.*

FDA Label Image

136 (Hydralazine Str)

Chemical structure of Hydralazine Hydrochloride, showing the molecular arrangement including a hydrazine group attached to a bicyclic ring system, along with the hydrochloride (HCl) component.*

* 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.