Package 0615-8346-39
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
0615-8346-39
Digits Only
0615834639
Product NDC
0615-8346
Description
30 TABLET in 1 BLISTER PACK (0615-8346-39)
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": "41a6941d-eb7b-4a2c-a46c-90e6e7b0aa2a", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["3eef522f-9e95-4668-bb12-09fd47ed0daf"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8346-39)", "package_ndc": "0615-8346-39", "marketing_start_date": "20200722"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "0615-8346_41a6941d-eb7b-4a2c-a46c-90e6e7b0aa2a", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0615-8346", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076690", "marketing_category": "ANDA", "marketing_start_date": "20060804", "listing_expiration_date": "20261231"}