Package 63629-2100-1

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-2100-1
Digits Only 6362921001
Product NDC 63629-2100
Product ID 63629-2100_c03a4815-4a12-4abb-aa11-0b1b078929da
Description

30 TABLET in 1 BOTTLE (63629-2100-1)

Marketing

Marketing Status
Marketed Since 2019-10-31
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": "c03a4815-4a12-4abb-aa11-0b1b078929da", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744"], "spl_set_id": ["5d184d1b-67fe-4965-bf3d-b49646df4f92"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-2100-1)", "package_ndc": "63629-2100-1", "marketing_start_date": "20191031"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "63629-2100_c03a4815-4a12-4abb-aa11-0b1b078929da", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63629-2100", "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": "150 mg/1"}], "application_number": "ANDA209193", "marketing_category": "ANDA", "marketing_start_date": "20191031", "listing_expiration_date": "20261231"}