Prazosin Hydrochloride Capsule
Product Images NDC 46708-692

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Prazosin Hydrochloride (NDC 46708-692). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic 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

100 Capsules (Prazosin Caps 1 mg)

Label for Prazosin Hydrochloride Capsules USP 1 mg by Alembic Pharmaceuticals Limited. The label shows that the package contains 100 oral capsules, Rx only, with storage instructions and manufacturing details from Alembic in Gujarat, India. It includes an NDC number 46708-691-31 and a barcode.*

FDA Label Image

100 Capsules (Prazosin Caps 2 mg)

Label for Prazosin Hydrochloride Capsules, USP, 2 mg strength by Alembic Pharmaceuticals Limited. The label indicates the product contains 100 capsules and is for prescription use only. Storage instructions specify maintaining 25°C with permitted excursions, and it notes the package is child-resistant. Manufacturer information and an NDC number are also included.*

FDA Label Image

100 Capsules (Prazosin Caps 5 mg)

Label for Prazosin Hydrochloride Capsules, USP 5 mg by Alembic Pharmaceuticals Limited. The label states the product is a prescription oral capsule, with 100 capsules per package. It includes storage instructions, manufacturer information, and a barcode, emphasizing child-resistant packaging and controlled room temperature storage.*

FDA Label Image

Structure (Prazosin Str)

Chemical structure diagram of Prazosin Hydrochloride showing its molecular arrangement including multiple rings and functional groups, depicted with standard chemical notation.*

* 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.