Package 46708-036-31

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 46708-036-31
Digits Only 4670803631
Product NDC 46708-036
Description

100 TABLET, FILM COATED in 1 BOTTLE (46708-036-31)

Marketing

Marketing Status
Marketed Since 2013-09-12
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aad4b153-ed5a-4781-ba0f-fb4bcf990057", "openfda": {"upc": ["0346708030315", "0346708033316", "0346708036317", "0346708034313", "0346708032319", "0346708035310", "0346708031312"], "unii": ["D7ZD41RZI9"], "rxcui": ["283858", "312845", "312846", "312847", "312849", "314208", "562704"], "spl_set_id": ["9a25f575-09ab-4d32-b73e-5426f08c00c4"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-036-31)", "package_ndc": "46708-036-31", "marketing_start_date": "20130912"}], "brand_name": "ROPINIROLE", "product_id": "46708-036_aad4b153-ed5a-4781-ba0f-fb4bcf990057", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "46708-036", "generic_name": "ROPINIROLE", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROPINIROLE", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090429", "marketing_category": "ANDA", "marketing_start_date": "20130912", "listing_expiration_date": "20261231"}