Package 11534-160-01

{"route": ["ORAL"], "spl_id": "a9fd0c08-60ae-4015-85c7-803989d00745", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803348", "803353"], "spl_set_id": ["43024f64-2d77-49a9-80fd-ad07a86c69a3"], "manufacturer_name": ["SUNRISE PHARMACEUTICAL, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (11534-160-01)", "package_ndc": "11534-160-01", "marketing_start_date": "20170124"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (11534-160-03)", "package_ndc": "11534-160-03", "marketing_start_date": "20170124"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (11534-160-30)", "package_ndc": "11534-160-30", "marketing_start_date": "20170124"}], "brand_name": "Phentermine hydrochloride", "product_id": "11534-160_a9fd0c08-60ae-4015-85c7-803989d00745", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "11534-160", "dea_schedule": "CIV", "generic_name": "phentermine hydrochloride", "labeler_name": "SUNRISE PHARMACEUTICAL, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA205008", "marketing_category": "ANDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}