Package 33342-195-10

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 33342-195-10
Digits Only 3334219510
Product NDC 33342-195
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-10)

Marketing

Marketing Status
Marketed Since 2018-08-14
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": "ea9c3795-420f-49fb-918c-7033a1f06963", "openfda": {"upc": ["0333342196071", "0333342196569", "0333342195074", "0333342196156", "0333342194152", "0333342194077"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["3e51f786-3691-4ec4-836b-7f2c9a385aa7"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-07)", "package_ndc": "33342-195-07", "marketing_start_date": "20171006"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-10)", "package_ndc": "33342-195-10", "marketing_start_date": "20180814"}, {"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-11)", "package_ndc": "33342-195-11", "marketing_start_date": "20180814"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-15)", "package_ndc": "33342-195-15", "marketing_start_date": "20171006"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-195-56)  / 14 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "33342-195-56", "marketing_start_date": "20171006"}], "brand_name": "Venlafaxine hydrochloride", "product_id": "33342-195_ea9c3795-420f-49fb-918c-7033a1f06963", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "33342-195", "generic_name": "Venlafaxine hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA204889", "marketing_category": "ANDA", "marketing_start_date": "20171006", "listing_expiration_date": "20261231"}