Package 50090-3205-0

{"route": ["ORAL"], "spl_id": "bb6e2af6-0020-470b-addb-df7bb4724ac7", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["3eb24fa9-921b-4bdb-9e0a-c82cb600df0f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-3205-0)", "package_ndc": "50090-3205-0", "marketing_start_date": "20171205"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-3205-1)", "package_ndc": "50090-3205-1", "marketing_start_date": "20171024"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "50090-3205_bb6e2af6-0020-470b-addb-df7bb4724ac7", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-3205", "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": "30 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}