Package 46708-266-30

Brand: ropinirole

Generic: ropinirole
NDC Package

Package Facts

Identity

Package NDC 46708-266-30
Digits Only 4670826630
Product NDC 46708-266
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-266-30)

Marketing

Marketing Status
Marketed Since 2013-03-14
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": "a1e5da4e-74fc-4482-8e15-599c665f2c2f", "openfda": {"upc": ["0346708263300", "0346708262303", "0346708264307", "0346708265304", "0346708266301"], "unii": ["D7ZD41RZI9"], "rxcui": ["799054", "799055", "799056", "824959", "848582"], "spl_set_id": ["2e01dbdd-f439-45d7-9085-2d92a1a1fee2"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (46708-266-10)", "package_ndc": "46708-266-10", "marketing_start_date": "20130314"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-266-30)", "package_ndc": "46708-266-30", "marketing_start_date": "20130314"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-266-31)", "package_ndc": "46708-266-31", "marketing_start_date": "20130314"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-266-71)", "package_ndc": "46708-266-71", "marketing_start_date": "20130314"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-266-90)", "package_ndc": "46708-266-90", "marketing_start_date": "20130314"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-266-91)", "package_ndc": "46708-266-91", "marketing_start_date": "20130314"}], "brand_name": "Ropinirole", "product_id": "46708-266_a1e5da4e-74fc-4482-8e15-599c665f2c2f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "46708-266", "generic_name": "Ropinirole", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "12 mg/1"}], "application_number": "ANDA202786", "marketing_category": "ANDA", "marketing_start_date": "20130314", "listing_expiration_date": "20261231"}