Package 71205-525-60

{"route": ["ORAL"], "spl_id": "4318dfda-092c-4ade-83c5-581bc968f391", "openfda": {"upc": ["0371205525309"], "unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["3dec1805-9a95-462e-8784-303004d500b1"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30)", "package_ndc": "71205-525-30", "marketing_start_date": "20210122"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60)", "package_ndc": "71205-525-60", "marketing_start_date": "20210122"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90)", "package_ndc": "71205-525-90", "marketing_start_date": "20210122"}], "brand_name": "Duloxetine", "product_id": "71205-525_4318dfda-092c-4ade-83c5-581bc968f391", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71205-525", "generic_name": "Duloxetine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20261231"}