Package 29300-155-19

{"route": ["ORAL"], "spl_id": "8190595a-be8e-4fd0-bcdf-30b6ba64ef5a", "openfda": {"unii": ["75046A1XTN"], "rxcui": ["861132"], "spl_set_id": ["644295a9-75cb-4326-a71f-b0f4e0c4cf75"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-155-01)", "package_ndc": "29300-155-01", "marketing_start_date": "20160315"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-155-13)", "package_ndc": "29300-155-13", "marketing_start_date": "20160315"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-155-19)", "package_ndc": "29300-155-19", "marketing_start_date": "20160315"}], "brand_name": "Alfuzosin hydrochloride", "product_id": "29300-155_8190595a-be8e-4fd0-bcdf-30b6ba64ef5a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "29300-155", "generic_name": "Alfuzosin hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alfuzosin hydrochloride", "active_ingredients": [{"name": "ALFUZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203192", "marketing_category": "ANDA", "marketing_start_date": "20160315", "listing_expiration_date": "20261231"}