Package 63629-9284-1

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-9284-1
Digits Only 6362992841
Product NDC 63629-9284
Product ID 63629-9284_cc13669d-53e1-4afa-97e7-55315e9f082c
Description

30 TABLET in 1 BOTTLE (63629-9284-1)

Marketing

Marketing Status
Marketed Since 2022-06-06
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cc13669d-53e1-4afa-97e7-55315e9f082c", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808748"], "spl_set_id": ["5c3536c6-8c80-4b41-bb9f-06731f4d3868"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-9284-1)", "package_ndc": "63629-9284-1", "marketing_start_date": "20220606"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "63629-9284_cc13669d-53e1-4afa-97e7-55315e9f082c", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63629-9284", "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": "225 mg/1"}], "application_number": "ANDA209193", "marketing_category": "ANDA", "marketing_start_date": "20191226", "listing_expiration_date": "20261231"}