Package 72205-052-30

{"route": ["ORAL"], "spl_id": "97c3bda8-3dbe-4c7a-aee9-00418c11d24c", "openfda": {"upc": ["0372205052918", "0372205052307", "0372205053915"], "unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["96086fd8-8fa3-4a2b-ac12-fe1a3ad4f384"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72205-052-05)", "package_ndc": "72205-052-05", "marketing_start_date": "20230405"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72205-052-30)", "package_ndc": "72205-052-30", "marketing_start_date": "20230405"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72205-052-91)", "package_ndc": "72205-052-91", "marketing_start_date": "20230405"}], "brand_name": "Doxepin hydrochloride", "product_id": "72205-052_97c3bda8-3dbe-4c7a-aee9-00418c11d24c", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72205-052", "generic_name": "Doxepin hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA214823", "marketing_category": "ANDA", "marketing_start_date": "20230405", "listing_expiration_date": "20261231"}