Package 31722-126-90

{"route": ["ORAL"], "spl_id": "495259b8-9f81-4b6e-aa51-d199aa0edfb8", "openfda": {"upc": ["0331722126908", "0331722125307", "0331722126304", "0331722123907", "0331722123303", "0331722124300", "0331722124904", "0331722125901"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd3"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-126-30)", "package_ndc": "31722-126-30", "marketing_start_date": "20201023"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-126-90)", "package_ndc": "31722-126-90", "marketing_start_date": "20201023"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "31722-126_495259b8-9f81-4b6e-aa51-d199aa0edfb8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "31722-126", "generic_name": "venlafaxine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA214419", "marketing_category": "ANDA", "marketing_start_date": "20201023", "listing_expiration_date": "20261231"}