Ropinirole Tablet, Film Coated, Extended Release
Product Images NDC 46708-264

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Ropinirole (NDC 46708-264). 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

Structure (Ropinirole Structure)

Chemical structure diagram of the active ingredient ropinirole, showing its molecular framework including a benzene ring, nitrogen atoms, and an attached side chain.*

FDA Label Image

2 mg 30's Hdpe Bottle Pack (Ropinirole 2mg)

Ropinirole Extended-Release Tablets label showing 2 mg strength. The label includes the NDC 46708-262-30 barcode, contains 30 tablets, and is manufactured by Alembic Pharmaceuticals Limited. It notes the active ingredient amount as 2.28 mg ropinirole hydrochloride equivalent to 2 mg ropinirole, with storage instructions and dispensing information for pharmacists.*

FDA Label Image

4 mg 30's Hdpe Bottle Pack (Ropinirole 4mg)

Ropinirole Extended-Release Tablets label showing 4 mg strength in a film-coated, extended-release oral tablet form. The label includes the NDC number 46708-263-30, manufacturer Alembic Pharmaceuticals Limited, and packaging for 30 tablets. It also contains dosage, storage instructions, and a barcode.*

FDA Label Image

6 mg 30's Hdpe Bottle Pack (Ropinirole 6mg)

Label for Ropinirole Extended-Release Tablets, 6 mg strength. The label indicates each extended-release tablet contains 6.84 mg ropinirole hydrochloride equivalent to 6 mg ropinirole. It is manufactured by Alembic Pharmaceuticals Limited and includes storage instructions and a note for pharmacists to dispense the patient information leaflet. The label also includes the NDC 46708-264-30 and barcode.*

FDA Label Image

8 mg 30's Hdpe Bottle Pack (Ropinirole 8mg)

Ropinirole Extended-Release Tablets, 8 mg strength, film-coated, for oral use. The label highlights the dosage strength prominently and includes instructions for pharmacists to dispense the patient information leaflet. It also provides storage conditions (20° to 25°C), safety warnings about the seal under the cap, batch and expiry fields, and manufacturer details for Alembic Pharmaceuticals Limited in India. The package contains 30 tablets and is Rx only.*

FDA Label Image

12 mg 30's Hdpe Bottle Pack (Ropinirole 12mg)

Label for Ropinirole Extended-Release Tablets, 12 mg strength, film-coated oral tablets. The label states 30 tablets per package and includes manufacturer information for Alembic Pharmaceuticals Limited. Dosage instructions and storage conditions are partially visible, along with the NDC number 46708-266-30 and a barcode.*

* 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.