Package 71335-1104-2

Brand: venlafaxine

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1104-2
Digits Only 7133511042
Product NDC 71335-1104
Description

30 TABLET in 1 BOTTLE (71335-1104-2)

Marketing

Marketing Status
Marketed Since 2019-02-13
Brand venlafaxine
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6feb7962-b69c-40d9-a853-f2ea11ae333f", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["304bda24-9151-47b5-9f62-005ea325a11e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1104-1)", "package_ndc": "71335-1104-1", "marketing_start_date": "20190220"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1104-2)", "package_ndc": "71335-1104-2", "marketing_start_date": "20190213"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1104-3)", "package_ndc": "71335-1104-3", "marketing_start_date": "20200103"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1104-4)", "package_ndc": "71335-1104-4", "marketing_start_date": "20211228"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1104-5)", "package_ndc": "71335-1104-5", "marketing_start_date": "20211228"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1104-6)", "package_ndc": "71335-1104-6", "marketing_start_date": "20211228"}], "brand_name": "venlafaxine", "product_id": "71335-1104_6feb7962-b69c-40d9-a853-f2ea11ae333f", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-1104", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20100407", "listing_expiration_date": "20261231"}