Package 70518-3790-0

{"route": ["ORAL"], "spl_id": "3b2789ab-f007-2d7f-e063-6294a90af15d", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["4cc3327b-92c5-4667-ae16-3e95eafcf4d8"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3790-0)", "package_ndc": "70518-3790-0", "marketing_start_date": "20230713"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3790-1)", "package_ndc": "70518-3790-1", "marketing_start_date": "20240607"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "70518-3790_3b2789ab-f007-2d7f-e063-6294a90af15d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "70518-3790", "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": "ANDA207479", "marketing_category": "ANDA", "marketing_start_date": "20230713", "listing_expiration_date": "20261231"}