Package 50268-742-15
Brand: ropinirole hydrochloride
Generic: ropinirole hydrochloridePackage Facts
Identity
Package NDC
50268-742-15
Digits Only
5026874215
Product NDC
50268-742
Description
50 BLISTER PACK in 1 BOX (50268-742-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-742-11)
Marketing
Marketing Status
Brand
ropinirole hydrochloride
Generic
ropinirole hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b4c1c97-dc70-3801-e063-6394a90a7faf", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["312845", "312846", "312847", "314208"], "spl_set_id": ["e699a31a-25fc-554b-e053-2a95a90a843a"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-742-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-742-11)", "package_ndc": "50268-742-15", "marketing_start_date": "20220819"}], "brand_name": "ropinirole hydrochloride", "product_id": "50268-742_2b4c1c97-dc70-3801-e063-6394a90a7faf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50268-742", "generic_name": "ropinirole hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ropinirole hydrochloride", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA078110", "marketing_category": "ANDA", "marketing_start_date": "20220819", "listing_expiration_date": "20261231"}