Package 71335-2779-2
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
71335-2779-2
Digits Only
7133527792
Product NDC
71335-2779
Description
60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2779-2)
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": "39978766-e2d0-4cd6-9ba0-dd64c44adfca", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["7aa3edba-4248-49bb-86f7-06fdbf2a6fb7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2779-1)", "package_ndc": "71335-2779-1", "marketing_start_date": "20251013"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2779-2)", "package_ndc": "71335-2779-2", "marketing_start_date": "20251013"}, {"sample": false, "description": "10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2779-3)", "package_ndc": "71335-2779-3", "marketing_start_date": "20251013"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2779-4)", "package_ndc": "71335-2779-4", "marketing_start_date": "20251013"}, {"sample": false, "description": "14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2779-5)", "package_ndc": "71335-2779-5", "marketing_start_date": "20251013"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "71335-2779_39978766-e2d0-4cd6-9ba0-dd64c44adfca", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-2779", "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": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}