Package 58657-649-01

{"route": ["ORAL"], "spl_id": "2ea9750b-e90d-cc5b-e063-6394a90a7e78", "openfda": {"unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["dffb5fdd-06c0-4275-9f89-9e12b3adf8a9"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58657-649-01)", "package_ndc": "58657-649-01", "marketing_start_date": "20200701"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (58657-649-10)", "package_ndc": "58657-649-10", "marketing_start_date": "20200701"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (58657-649-50)", "package_ndc": "58657-649-50", "marketing_start_date": "20200701"}], "brand_name": "Clonidine Hydrochloride", "product_id": "58657-649_2ea9750b-e90d-cc5b-e063-6394a90a7e78", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "58657-649", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clonidine Hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA202297", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}