Bromocriptine Mesylate
Product Images NDC 63304-158

3 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bromocriptine Mesylate (NDC 63304-158). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Structure (Bromocriptine 01)

Structure (Bromocriptine 01)
Chemical structure diagram of BROMIPTINE MESYLATE, showing the molecular formula C32H40BrN5O5 with methanesulfonic acid (CH4SO3) and a molecular weight of 750.70.*
FDA Label Image

R:\regulatory\spl\jennifer\bromocriptine\pictures\bromocriptine-02.jpg (Bromocriptine 02)

R:\regulatory\spl\jennifer\bromocriptine\pictures\bromocriptine-02.jpg (Bromocriptine 02)
Label for Bromocriptine Mesylate Tablets USP 2.5 mg by Sun Pharmaceutical Industries, Inc. The label states the product contains 30 tablets, is Rx only, and provides storage instructions. It includes a barcode, NDC number 63304-962-30, and distributor information for Sun Pharmaceutical Industries and manufacturer details for Sun Pharmaceutical Laboratories.*
FDA Label Image

Bromocriptine 03

Bromocriptine 03
Label for Bromocriptine Mesylate Capsules, USP 5 mg, containing 30 capsules. The label includes the NDC 63304-158-30 and indicates it is for prescription use only. Distributed by Sun Pharmaceutical Industries, Inc., with manufacturing and packaging details provided. Storage and dispensing instructions are partially visible.*

* 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.