Package 67877-729-30

{"route": ["ORAL"], "spl_id": "17943f8a-6ea6-4e86-93cc-df580774a8d9", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["528d5392-4ad5-48c5-963d-6ebfb9187db4"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-729-30)", "package_ndc": "67877-729-30", "marketing_start_date": "20210611"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-729-90)", "package_ndc": "67877-729-90", "marketing_start_date": "20210611"}], "brand_name": "Venlafaxine", "product_id": "67877-729_17943f8a-6ea6-4e86-93cc-df580774a8d9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "67877-729", "generic_name": "Venlafaxine", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA214127", "marketing_category": "ANDA", "marketing_start_date": "20210611", "listing_expiration_date": "20261231"}