Package 47335-738-88

{"route": ["ORAL"], "spl_id": "b8e6ae63-c5d7-4481-b7b0-17e135670515", "openfda": {"upc": ["0347335738865", "0347335737868"], "unii": ["ZG7E5POY8O"], "rxcui": ["993503", "993518", "993536"], "spl_set_id": ["29848192-7de3-4c0d-a822-1268dcf128b0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-08)", "package_ndc": "47335-738-08", "marketing_start_date": "20200301"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-13)", "package_ndc": "47335-738-13", "marketing_start_date": "20200301"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-86)", "package_ndc": "47335-738-86", "marketing_start_date": "20200301"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-738-88)", "package_ndc": "47335-738-88", "marketing_start_date": "20200301"}], "brand_name": "Bupropion hydrochloride", "product_id": "47335-738_b8e6ae63-c5d7-4481-b7b0-17e135670515", "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": "47335-738", "generic_name": "Bupropion hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA078866", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}