Package 55111-547-90

{"route": ["ORAL"], "spl_id": "20a19933-a7c1-3739-c472-272204375d1e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["106d0d7b-925b-74e7-83cb-562144ce1f92"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-547-01)", "package_ndc": "55111-547-01", "marketing_start_date": "20080616"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-547-05)", "package_ndc": "55111-547-05", "marketing_start_date": "20080616"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-547-30)", "package_ndc": "55111-547-30", "marketing_start_date": "20080616"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55111-547-60)", "package_ndc": "55111-547-60", "marketing_start_date": "20080616"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (55111-547-79)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "55111-547-79", "marketing_start_date": "20080616"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55111-547-90)", "package_ndc": "55111-547-90", "marketing_start_date": "20080616"}], "brand_name": "Venlafaxine hydrochloride", "product_id": "55111-547_20a19933-a7c1-3739-c472-272204375d1e", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "55111-547", "generic_name": "Venlafaxine hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA078301", "marketing_category": "ANDA", "marketing_start_date": "20080616", "listing_expiration_date": "20261231"}