Package 57664-393-88

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 57664-393-88
Digits Only 5766439388
Product NDC 57664-393
Description

100 TABLET in 1 BOTTLE (57664-393-88)

Marketing

Marketing Status
Marketed Since 2008-06-13
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": "4a916be7-abd4-8771-e063-6394a90a86eb", "openfda": {"upc": ["0357664393888", "0357664396889", "0357664394885", "0357664392881"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["55889b3d-74c9-4638-9a14-6a4ca3a99f7f"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (57664-393-88)", "package_ndc": "57664-393-88", "marketing_start_date": "20080613"}], "brand_name": "Venlafaxine", "product_id": "57664-393_4a916be7-abd4-8771-e063-6394a90a86eb", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "57664-393", "generic_name": "Venlafaxine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA078627", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20271231"}