Package 50090-6889-0

{"route": ["ORAL"], "spl_id": "2bcd10f1-d5c6-4886-ac10-39e7a658448d", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["be33f3cb-6fd1-4377-816e-84bd49370e9e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-0)", "package_ndc": "50090-6889-0", "marketing_start_date": "20231206"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-1)", "package_ndc": "50090-6889-1", "marketing_start_date": "20231206"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "50090-6889_2bcd10f1-d5c6-4886-ac10-39e7a658448d", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-6889", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "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": "20140611", "listing_expiration_date": "20261231"}