Package 82804-038-60

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-038-60
Digits Only 8280403860
Product NDC 82804-038
Description

60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-60)

Marketing

Marketing Status
Marketed Since 2023-11-07
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": "5c558ab8-b4b3-4973-b016-ed5cfcb4d88b", "openfda": {"upc": ["0382804038305"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["5c558ab8-b4b3-4973-b016-ed5cfcb4d88b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-30)", "package_ndc": "82804-038-30", "marketing_start_date": "20231107"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-60)", "package_ndc": "82804-038-60", "marketing_start_date": "20231107"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-90)", "package_ndc": "82804-038-90", "marketing_start_date": "20231107"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "82804-038_5c558ab8-b4b3-4973-b016-ed5cfcb4d88b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "82804-038", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20111123", "listing_expiration_date": "20261231"}