Package 43063-633-90

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 43063-633-90
Digits Only 4306363390
Product NDC 43063-633
Description

90 TABLET in 1 BOTTLE, PLASTIC (43063-633-90)

Marketing

Marketing Status
Marketed Since 2015-11-25
Brand venlafaxine
Generic venlafaxine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4139d5c9-2e2b-7f2d-e063-6394a90a35e6", "openfda": {"upc": ["0343063633908"], "unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["18495527-add4-42a5-bbf7-9f8dc2df06af"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-633-90)", "package_ndc": "43063-633-90", "marketing_start_date": "20151125"}], "brand_name": "Venlafaxine", "product_id": "43063-633_4139d5c9-2e2b-7f2d-e063-6394a90a35e6", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43063-633", "generic_name": "Venlafaxine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078627", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}