Package 50771-202-01

{"route": ["ORAL"], "spl_id": "4502c810-4eb5-29c4-e063-6394a90aefe4", "openfda": {"upc": ["0350771203019", "0350771202012", "0350771201015"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["90224073-178d-7ec5-e053-2995a90a20fc"], "manufacturer_name": ["Yaopharma Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-202-01)", "package_ndc": "50771-202-01", "marketing_start_date": "20240101"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-202-02)", "package_ndc": "50771-202-02", "marketing_start_date": "20240101"}], "brand_name": "DULOXETINE HYDROCHLORIDE", "product_id": "50771-202_4502c810-4eb5-29c4-e063-6394a90aefe4", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50771-202", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Yaopharma Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DULOXETINE HYDROCHLORIDE", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA207219", "marketing_category": "ANDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}