Package 31722-170-90

{"route": ["ORAL"], "spl_id": "232a4dda-8bb0-52fa-e063-6394a90ab09e", "openfda": {"upc": ["0331722169301", "0331722168601", "0331722170307"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["b14feecc-04c6-4b2d-ba55-2e1dbef6b0d7"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-01)", "package_ndc": "31722-170-01", "marketing_start_date": "20201230"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-10)", "package_ndc": "31722-170-10", "marketing_start_date": "20201230"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-30)", "package_ndc": "31722-170-30", "marketing_start_date": "20201230"}, {"sample": false, "description": "7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-170-31)", "package_ndc": "31722-170-31", "marketing_start_date": "20201230"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-90)", "package_ndc": "31722-170-90", "marketing_start_date": "20240629"}], "brand_name": "Duloxetine", "product_id": "31722-170_232a4dda-8bb0-52fa-e063-6394a90ab09e", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "31722-170", "generic_name": "Duloxetine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204343", "marketing_category": "ANDA", "marketing_start_date": "20201230", "listing_expiration_date": "20261231"}