Package 29300-419-10

{"route": ["ORAL"], "spl_id": "3f6bcdb5-c8ad-45c0-b43f-2dbea8980376", "openfda": {"upc": ["0329300420012"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["9c6e0e05-b579-4fae-b768-e1a664c39bb8"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (29300-419-01)", "package_ndc": "29300-419-01", "marketing_start_date": "20210526"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (29300-419-05)", "package_ndc": "29300-419-05", "marketing_start_date": "20210526"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (29300-419-10)", "package_ndc": "29300-419-10", "marketing_start_date": "20211116"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "29300-419_3f6bcdb5-c8ad-45c0-b43f-2dbea8980376", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "29300-419", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}