Package 62332-317-30

{"route": ["ORAL"], "spl_id": "06c52509-29c8-41c5-8492-3458df75f3d5", "openfda": {"upc": ["0362332320318"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["cad14805-64d8-4257-b5f1-d56e0063f0e2"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-317-30)", "package_ndc": "62332-317-30", "marketing_start_date": "20210708"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-317-31)", "package_ndc": "62332-317-31", "marketing_start_date": "20210708"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-317-91)", "package_ndc": "62332-317-91", "marketing_start_date": "20210708"}], "brand_name": "DESIPRAMINE HYDROCHLORIDE", "product_id": "62332-317_06c52509-29c8-41c5-8492-3458df75f3d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "62332-317", "generic_name": "DESIPRAMINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA209785", "marketing_category": "ANDA", "marketing_start_date": "20210708", "listing_expiration_date": "20261231"}