Package 50771-001-02

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50771-001-02
Digits Only 5077100102
Product NDC 50771-001
Product ID 50771-001_4502de86-571d-cfb3-e063-6294a90a34f8
Description

100 TABLET in 1 BOTTLE, PLASTIC (50771-001-02)

Marketing

Marketing Status
Marketed Since 2016-09-06
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": "4502de86-571d-cfb3-e063-6294a90a34f8", "openfda": {"upc": ["0350771003022", "0350771002025", "0350771001028", "0350771004029"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["38fd2c97-cd30-2f7d-e054-00144ff8d46c"], "manufacturer_name": ["Yaopharma Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (50771-001-02)", "package_ndc": "50771-001-02", "marketing_start_date": "20160906"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50771-001_4502de86-571d-cfb3-e063-6294a90a34f8", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50771-001", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Yaopharma Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA202036", "marketing_category": "ANDA", "marketing_start_date": "20160906", "listing_expiration_date": "20261231"}