Package 64980-579-09

Brand: venlafaxine hydrochloride

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 64980-579-09
Digits Only 6498057909
Product NDC 64980-579
Product ID 64980-579_7f187899-ddc6-4e15-b2af-e54f59d5baf4
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-579-09)

Marketing

Marketing Status
Marketed Since 2022-11-28
Brand venlafaxine hydrochloride
Generic venlafaxine
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": "7f187899-ddc6-4e15-b2af-e54f59d5baf4", "openfda": {"upc": ["0364980578035", "0364980579032", "0364980581035", "0364980580038"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["074f4478-e81b-45a2-ae85-ffd27bed940f"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-579-03)", "package_ndc": "64980-579-03", "marketing_start_date": "20221128"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-579-09)", "package_ndc": "64980-579-09", "marketing_start_date": "20221128"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "64980-579_7f187899-ddc6-4e15-b2af-e54f59d5baf4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "64980-579", "generic_name": "Venlafaxine", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA216044", "marketing_category": "ANDA", "marketing_start_date": "20221128", "listing_expiration_date": "20261231"}