Package 0591-3543-60

{"route": ["ORAL"], "spl_id": "7f46f208-d4e4-415a-a5e7-2afeea280d05", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["1801289"], "spl_set_id": ["a591e33a-52f0-41c8-a00b-4a1afcc3dc4c"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3543-60)", "package_ndc": "0591-3543-60", "marketing_start_date": "20090611"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0591-3543-76)  / 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "0591-3543-76", "marketing_start_date": "20090825"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "0591-3543_7f46f208-d4e4-415a-a5e7-2afeea280d05", "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": "0591-3543", "generic_name": "bupropion hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA079094", "marketing_category": "ANDA", "marketing_start_date": "20090611", "listing_expiration_date": "20271231"}