Package 76420-672-60

{"route": ["ORAL"], "spl_id": "1244caf6-4ab7-dd22-e063-6294a90a81bd", "openfda": {"unii": ["6E8ZO8LRNM"], "rxcui": ["856364", "856369", "856373", "856377"], "spl_set_id": ["04a676ee-358e-484d-9de4-a9a88d908ba8"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-672-01)", "package_ndc": "76420-672-01", "marketing_start_date": "20240226"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-672-30)", "package_ndc": "76420-672-30", "marketing_start_date": "20240226"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-672-60)", "package_ndc": "76420-672-60", "marketing_start_date": "20240226"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-672-90)", "package_ndc": "76420-672-90", "marketing_start_date": "20240226"}], "brand_name": "Trazodone Hydrochloride", "product_id": "76420-672_1244caf6-4ab7-dd22-e063-6294a90a81bd", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "76420-672", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA205253", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}