Package 51655-849-26

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-849-26
Digits Only 5165584926
Product NDC 51655-849
Product ID 51655-849_4973e59c-ca21-14bf-e063-6394a90ade72
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-849-26)

Marketing

Marketing Status
Marketed Since 2023-02-03
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": "4973e59c-ca21-14bf-e063-6394a90ade72", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["f757cac4-efa7-668c-e053-6294a90a720d"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-849-26)", "package_ndc": "51655-849-26", "marketing_start_date": "20230203"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "51655-849_4973e59c-ca21-14bf-e063-6394a90ade72", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "51655-849", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20230203", "listing_expiration_date": "20271231"}