Package 13811-713-90
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
13811-713-90
Digits Only
1381171390
Product NDC
13811-713
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-713-90)
Marketing
Marketing Status
Brand
venlafaxine hydrochloride
Generic
venlafaxine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "55564637-0e7a-4684-be84-9d8c4cecacc3", "openfda": {"upc": ["0313811715309", "0313811714302", "0313811715903", "0313811713305", "0313811714906", "0313811712902", "0313811713909", "0313811712308"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["fdaed1c2-dd0a-4bf3-975a-86fe3e7f0c97"], "manufacturer_name": ["Trigen Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-713-30)", "package_ndc": "13811-713-30", "marketing_end_date": "20260531", "marketing_start_date": "20100429"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-713-90)", "package_ndc": "13811-713-90", "marketing_end_date": "20260531", "marketing_start_date": "20100429"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "13811-713_55564637-0e7a-4684-be84-9d8c4cecacc3", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "13811-713", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Trigen Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "NDA022104", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260531", "marketing_start_date": "20100429"}