Package 63187-414-60

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 63187-414-60
Digits Only 6318741460
Product NDC 63187-414
Description

60 TABLET in 1 BOTTLE (63187-414-60)

Marketing

Marketing Status
Marketed Since 2019-01-01
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": "36330e72-68ba-4393-b1f2-fd064d4e25cf", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["b5fc0187-590c-4bb9-a910-821eb0dc1fc8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-414-30)", "package_ndc": "63187-414-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-414-60)", "package_ndc": "63187-414-60", "marketing_start_date": "20190101"}], "brand_name": "Venlafaxine", "product_id": "63187-414_36330e72-68ba-4393-b1f2-fd064d4e25cf", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63187-414", "generic_name": "Venlafaxine", "labeler_name": "Proficient Rx LP", "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": "20080613", "listing_expiration_date": "20261231"}