Package 68084-856-01

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 68084-856-01
Digits Only 6808485601
Product NDC 68084-856
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01) / 1 TABLET in 1 BLISTER PACK (68084-856-11)

Marketing

Marketing Status
Marketed Since 2015-03-06
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": "1f401c77-b3c1-291d-e063-6394a90aa890", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313582", "313584", "313586"], "spl_set_id": ["d8899628-6e1b-40c6-9bc8-553d91ae2d0c"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-856-01)  / 1 TABLET in 1 BLISTER PACK (68084-856-11)", "package_ndc": "68084-856-01", "marketing_start_date": "20150306"}], "brand_name": "Venlafaxine", "product_id": "68084-856_1f401c77-b3c1-291d-e063-6394a90aa890", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68084-856", "generic_name": "Venlafaxine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20150306", "listing_expiration_date": "20261231"}