Package 81469-415-01

{"route": ["ORAL"], "spl_id": "55da757c-42d2-4963-b06f-def9f18a423f", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["3d4f84a4-07a1-4d0e-85f5-dcd43b236a42"], "manufacturer_name": ["First Nation Group, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (81469-415-01)", "package_ndc": "81469-415-01", "marketing_start_date": "20230111"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (81469-415-05)", "package_ndc": "81469-415-05", "marketing_start_date": "20230111"}], "brand_name": "Doxepin Hydrochloride", "product_id": "81469-415_55da757c-42d2-4963-b06f-def9f18a423f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "81469-415", "generic_name": "doxepin hydrochloride", "labeler_name": "First Nation Group, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA215710", "marketing_category": "ANDA", "marketing_start_date": "20230111", "listing_expiration_date": "20261231"}