Package 71610-739-33

{"route": ["ORAL"], "spl_id": "14c0b109-4960-6df5-e063-6394a90a4c51", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["b1f1345c-3b7f-4228-b7b7-b9a4648050e5"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "6000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-16)", "package_ndc": "71610-739-16", "marketing_start_date": "20240108"}, {"sample": false, "description": "840 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-33)", "package_ndc": "71610-739-33", "marketing_start_date": "20240322"}, {"sample": false, "description": "500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-74)", "package_ndc": "71610-739-74", "marketing_start_date": "20230927"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "71610-739_14c0b109-4960-6df5-e063-6394a90a4c51", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-739", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}