Package 71205-369-60

{"route": ["ORAL"], "spl_id": "61d97d27-06ed-49a4-9514-f02684521d4b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["18e77a42-6552-4042-9ed3-046c94f4f921"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-369-30)", "package_ndc": "71205-369-30", "marketing_start_date": "20191203"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-369-60)", "package_ndc": "71205-369-60", "marketing_start_date": "20191203"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-369-90)", "package_ndc": "71205-369-90", "marketing_start_date": "20191203"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "71205-369_61d97d27-06ed-49a4-9514-f02684521d4b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71205-369", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}