Package 68788-7935-6

{"route": ["ORAL"], "spl_id": "20a803f1-b6c5-45bb-9cdc-69f3917dd57a", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["e86eb765-ac9c-4ed9-bce8-819151559394"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-3)", "package_ndc": "68788-7935-3", "marketing_start_date": "20210615"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-6)", "package_ndc": "68788-7935-6", "marketing_start_date": "20210615"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-9)", "package_ndc": "68788-7935-9", "marketing_start_date": "20210615"}], "brand_name": "Duloxetine", "product_id": "68788-7935_20a803f1-b6c5-45bb-9cdc-69f3917dd57a", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-7935", "generic_name": "Duloxetine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20210615", "listing_expiration_date": "20261231"}