Package 70771-1529-1

{"route": ["ORAL"], "spl_id": "2a2843b4-5867-4df6-af9a-dbe0264d6f1b", "openfda": {"upc": ["0372578182069", "0372578181062"], "unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["1461ede6-24f0-42a1-b801-0cf4ef404985"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1529-0)", "package_ndc": "70771-1529-0", "marketing_start_date": "20240630"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1529-1)", "package_ndc": "70771-1529-1", "marketing_start_date": "20240630"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1529-3)", "package_ndc": "70771-1529-3", "marketing_start_date": "20240630"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1529-4)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "70771-1529-4", "marketing_start_date": "20240630"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1529-5)", "package_ndc": "70771-1529-5", "marketing_start_date": "20240630"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70771-1529-9)", "package_ndc": "70771-1529-9", "marketing_start_date": "20240630"}], "brand_name": "doxepin", "product_id": "70771-1529_2a2843b4-5867-4df6-af9a-dbe0264d6f1b", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70771-1529", "generic_name": "doxepin", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA202761", "marketing_category": "ANDA", "marketing_start_date": "20240630", "listing_expiration_date": "20261231"}