Package 33342-210-12

{"route": ["ORAL"], "spl_id": "4bae794e-6b1f-4630-9d00-a4524fffa0b9", "openfda": {"upc": ["0333342209078", "0333342214072", "0333342212122", "0333342210074", "0333342208071", "0333342211071", "0333342213075"], "unii": ["3D867NP06J"], "rxcui": ["901534", "901541", "901546", "901550", "901555", "1114479", "1114485"], "spl_set_id": ["1dbb8d2f-e0d9-4f8b-89d2-2a03496ef7be"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-210-07)", "package_ndc": "33342-210-07", "marketing_start_date": "20200824"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-210-12)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "33342-210-12", "marketing_start_date": "20200824"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "33342-210_4bae794e-6b1f-4630-9d00-a4524fffa0b9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "33342-210", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "1.5 mg/1"}], "application_number": "ANDA206156", "marketing_category": "ANDA", "marketing_start_date": "20200824", "listing_expiration_date": "20261231"}