Package 71335-9705-2
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
71335-9705-2
Digits Only
7133597052
Product NDC
71335-9705
Description
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9705-2)
Marketing
Marketing Status
Brand
venlafaxine hydrochloride
Generic
venlafaxine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ad82f38-f5da-4c97-b841-9a0b25236672", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["d7d1319c-500e-4ca0-83a1-a739cfa01cf7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9705-1)", "package_ndc": "71335-9705-1", "marketing_start_date": "20230602"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9705-2)", "package_ndc": "71335-9705-2", "marketing_start_date": "20230816"}, {"sample": false, "description": "10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9705-3)", "package_ndc": "71335-9705-3", "marketing_start_date": "20240716"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9705-4)", "package_ndc": "71335-9705-4", "marketing_start_date": "20230703"}, {"sample": false, "description": "14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9705-5)", "package_ndc": "71335-9705-5", "marketing_start_date": "20240716"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "71335-9705_4ad82f38-f5da-4c97-b841-9a0b25236672", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-9705", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20220907", "listing_expiration_date": "20271231"}