Package 72162-1599-1

{"route": ["ORAL"], "spl_id": "7a0ab4db-866d-4ff1-82d7-9616b57409bb", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["a23e79b3-7bd3-4b83-beb0-dc23d4830e9e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1599-1)", "package_ndc": "72162-1599-1", "marketing_start_date": "20240205"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1599-9)", "package_ndc": "72162-1599-9", "marketing_start_date": "20240205"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "72162-1599_7a0ab4db-866d-4ff1-82d7-9616b57409bb", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72162-1599", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}