Package 68788-7897-6

{"route": ["ORAL"], "spl_id": "8facbf87-c840-46ba-b14e-95b4e461a9e7", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["29eacc40-cbec-4cc9-8556-773346617e85"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-3)", "package_ndc": "68788-7897-3", "marketing_start_date": "20210514"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-6)", "package_ndc": "68788-7897-6", "marketing_start_date": "20210514"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7897-9)", "package_ndc": "68788-7897-9", "marketing_start_date": "20210514"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "68788-7897_8facbf87-c840-46ba-b14e-95b4e461a9e7", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-7897", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20210514", "listing_expiration_date": "20261231"}