Package 64850-251-30
Brand: ropinirole
Generic: ropinirolePackage Facts
Identity
Package NDC
64850-251-30
Digits Only
6485025130
Product NDC
64850-251
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-251-30)
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": "0ca68ebf-b908-4be4-a1a0-f9b3359375a4", "openfda": {"upc": ["0364850251303", "0364850254304", "0364850252300", "0364850253307", "0364850250306"], "unii": ["D7ZD41RZI9"], "rxcui": ["799054", "799055", "799056", "824959", "848582"], "spl_set_id": ["307411be-1c4e-44f7-b94d-737a3384c107"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64850-251-30)", "package_ndc": "64850-251-30", "marketing_start_date": "20251110"}], "brand_name": "Ropinirole", "product_id": "64850-251_0ca68ebf-b908-4be4-a1a0-f9b3359375a4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "64850-251", "generic_name": "Ropinirole", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropinirole", "active_ingredients": [{"name": "ROPINIROLE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA217862", "marketing_category": "ANDA", "marketing_start_date": "20251110", "listing_expiration_date": "20261231"}