Package 70518-4014-1

{"route": ["ORAL"], "spl_id": "390644de-7fad-5c4c-e063-6294a90a5f82", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["02275c51-6b3e-434a-bdb5-99135e73f1a4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-0)", "package_ndc": "70518-4014-0", "marketing_start_date": "20240207"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-1)", "package_ndc": "70518-4014-1", "marketing_start_date": "20250703"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "70518-4014_390644de-7fad-5c4c-e063-6294a90a5f82", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "70518-4014", "generic_name": "bupropion hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "XL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA210015", "marketing_category": "ANDA", "marketing_start_date": "20240207", "listing_expiration_date": "20261231"}