Package 71335-2515-3

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 71335-2515-3
Digits Only 7133525153
Product NDC 71335-2515
Product ID 71335-2515_59b4ff27-308c-4a28-810f-946f584d06d5
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-3)

Marketing

Marketing Status
Marketed Since 2024-10-24
Brand ropinirole
Generic ropinirole
Sample Package No

Linked Drug Pages (1)

Ropinirole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "59b4ff27-308c-4a28-810f-946f584d06d5", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312847"], "spl_set_id": ["af340f28-92b2-49af-b651-b9b01ca3ce6c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-1)", "package_ndc": "71335-2515-1", "marketing_start_date": "20241024"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-2)", "package_ndc": "71335-2515-2", "marketing_start_date": "20241024"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-3)", "package_ndc": "71335-2515-3", "marketing_start_date": "20241024"}], "brand_name": "Ropinirole", "product_id": "71335-2515_59b4ff27-308c-4a28-810f-946f584d06d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "71335-2515", "generic_name": "Ropinirole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA079229", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}