Package 0093-7385-56

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-7385-56
Digits Only 0093738556
Product NDC 0093-7385
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7385-56)

Marketing

Marketing Status
Marketed Since 2010-07-01
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": "4c5ca171-2a1c-4687-adf9-6d272463de4a", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["9a30e1b5-272b-4109-ad6c-a3c9a895822f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7385-05)", "package_ndc": "0093-7385-05", "marketing_start_date": "20120301"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7385-56)", "package_ndc": "0093-7385-56", "marketing_start_date": "20100701"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7385-98)", "package_ndc": "0093-7385-98", "marketing_start_date": "20100701"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "0093-7385_4c5ca171-2a1c-4687-adf9-6d272463de4a", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0093-7385", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076565", "marketing_category": "ANDA", "marketing_start_date": "20100701", "listing_expiration_date": "20271231"}