Package 68001-156-00
Brand: venlafaxine
Generic: venlafaxinePackage Facts
Identity
Package NDC
68001-156-00
Digits Only
6800115600
Product NDC
68001-156
Description
100 TABLET in 1 BOTTLE (68001-156-00)
Marketing
Marketing Status
Brand
venlafaxine
Generic
venlafaxine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04c5d11d-d249-eb93-e063-6294a90a1b46", "openfda": {"upc": ["0368001156004", "0368001157001", "0368001160001", "0368001158008", "0368001159005"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["172b3d3d-bdae-47bf-8fba-edd6da1a8649"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-156-00)", "package_ndc": "68001-156-00", "marketing_start_date": "20131125"}], "brand_name": "Venlafaxine", "product_id": "68001-156_04c5d11d-d249-eb93-e063-6294a90a1b46", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68001-156", "generic_name": "Venlafaxine", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20131125", "listing_expiration_date": "20261231"}