Package 71335-9605-1

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-9605-1
Digits Only 7133596051
Product NDC 71335-9605
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-1)

Marketing

Marketing Status
Marketed Since 2023-04-06
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": "cf86ed39-0f0a-4666-a225-9c50044e249e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["baae24d6-e425-4cfc-9a53-3cd223b6d344"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-1)", "package_ndc": "71335-9605-1", "marketing_start_date": "20230406"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-2)", "package_ndc": "71335-9605-2", "marketing_start_date": "20221128"}, {"sample": false, "description": "10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-3)", "package_ndc": "71335-9605-3", "marketing_start_date": "20240906"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-4)", "package_ndc": "71335-9605-4", "marketing_start_date": "20230104"}, {"sample": false, "description": "14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-5)", "package_ndc": "71335-9605-5", "marketing_start_date": "20240906"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "71335-9605_cf86ed39-0f0a-4666-a225-9c50044e249e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-9605", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20190708", "listing_expiration_date": "20261231"}