Package 76420-236-90

{"route": ["ORAL"], "spl_id": "e347f58a-9f2f-7e64-e053-2a95a90a528b", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["7c755ca3-0855-4b54-80a8-01b85f8e644a"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-30)", "package_ndc": "76420-236-30", "marketing_start_date": "20220707"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-60)", "package_ndc": "76420-236-60", "marketing_start_date": "20220707"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-90)", "package_ndc": "76420-236-90", "marketing_start_date": "20220707"}], "brand_name": "Duloxetine", "product_id": "76420-236_e347f58a-9f2f-7e64-e053-2a95a90a528b", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "76420-236", "generic_name": "Duloxetine", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20261231"}