Package 69452-358-20
Brand: ropinirole
Generic: ropinirolePackage Facts
Identity
Package NDC
69452-358-20
Digits Only
6945235820
Product NDC
69452-358
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-358-20)
Marketing
Marketing Status
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": "fa1451cc-4c3a-4f53-a848-685a3e5d9f89", "openfda": {"unii": ["D7ZD41RZI9"], "rxcui": ["283858", "312845", "312846", "312847", "312849", "314208", "562704"], "spl_set_id": ["4e6b070c-50a6-4742-af3c-59b45c45735e"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-358-20)", "package_ndc": "69452-358-20", "marketing_start_date": "20220915"}], "brand_name": "Ropinirole", "product_id": "69452-358_fa1451cc-4c3a-4f53-a848-685a3e5d9f89", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "69452-358", "generic_name": "Ropinirole", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA079229", "marketing_category": "ANDA", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}