Package 0093-9147-01

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-9147-01
Digits Only 0093914701
Product NDC 0093-9147
Product ID 0093-9147_da23a2ab-f20e-4208-b72b-d50260b97923
Description

100 TABLET in 1 BOTTLE (0093-9147-01)

Marketing

Marketing Status
Marketed Since 2006-08-04
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
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": "da23a2ab-f20e-4208-b72b-d50260b97923", "openfda": {"upc": ["0300939148010", "0300939149017", "0300939163013", "0300939147013", "0300939157012"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["37aaa8ac-4e0c-4e04-98b5-19b0d90d857c"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-9147-01)", "package_ndc": "0093-9147-01", "marketing_start_date": "20060804"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "0093-9147_da23a2ab-f20e-4208-b72b-d50260b97923", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0093-9147", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA076690", "marketing_category": "ANDA", "marketing_start_date": "20060804", "listing_expiration_date": "20261231"}