Package 50090-6406-1

{"route": ["ORAL"], "spl_id": "eaec6517-6ac0-4432-bbb6-9b3c70e7a1d9", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["2be9e5fb-011e-424b-b504-df2a28b5271d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6406-0)", "package_ndc": "50090-6406-0", "marketing_start_date": "20230323"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6406-1)", "package_ndc": "50090-6406-1", "marketing_start_date": "20230724"}], "brand_name": "Duloxetine", "product_id": "50090-6406_eaec6517-6ac0-4432-bbb6-9b3c70e7a1d9", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-6406", "generic_name": "Duloxetine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}