Package 51407-207-30

{"route": ["ORAL"], "spl_id": "447188f5-1076-885a-e063-6294a90ae7c5", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541", "993557"], "spl_set_id": ["8722a60e-7635-7455-e053-2991aa0abaf7"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-207-30)", "package_ndc": "51407-207-30", "marketing_start_date": "20190225"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51407-207-90)", "package_ndc": "51407-207-90", "marketing_start_date": "20190225"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "51407-207_447188f5-1076-885a-e063-6294a90ae7c5", "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": "51407-207", "generic_name": "bupropion hydrochloride", "labeler_name": "Golden State Medical Supply, 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": "ANDA210081", "marketing_category": "ANDA", "marketing_start_date": "20171103", "listing_expiration_date": "20261231"}