Package 82009-058-05

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82009-058-05
Digits Only 8200905805
Product NDC 82009-058
Product ID 82009-058_b5d4c4fe-1c29-466a-9ca6-6267c7a954eb
Description

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82009-058-05)

Marketing

Marketing Status
Marketed Since 2022-11-21
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": "b5d4c4fe-1c29-466a-9ca6-6267c7a954eb", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["cb4c04a6-47d1-44ff-8d58-718102fa08eb"], "manufacturer_name": ["QUALLENT PHARMACEUTICALS HEALTH LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82009-058-05)", "package_ndc": "82009-058-05", "marketing_start_date": "20221121"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "82009-058_b5d4c4fe-1c29-466a-9ca6-6267c7a954eb", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "82009-058", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "QUALLENT PHARMACEUTICALS HEALTH LLC", "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": "20221121", "listing_expiration_date": "20261231"}