Package 51655-223-52
Brand: venlafaxine
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
51655-223-52
Digits Only
5165522352
Product NDC
51655-223
Description
30 TABLET in 1 BOTTLE, PLASTIC (51655-223-52)
Marketing
Marketing Status
Brand
venlafaxine
Generic
venlafaxine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d2b0e8-15c2-b31b-e063-6294a90a08a6", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["f2b5c729-17c8-7ecc-e053-2a95a90a2e53"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-223-26)", "package_ndc": "51655-223-26", "marketing_start_date": "20230227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-223-52)", "package_ndc": "51655-223-52", "marketing_start_date": "20221025"}], "brand_name": "venlafaxine", "product_id": "51655-223_48d2b0e8-15c2-b31b-e063-6294a90a08a6", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "51655-223", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20221025", "listing_expiration_date": "20271231"}