Package 68788-6806-9
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
68788-6806-9
Digits Only
6878868069
Product NDC
68788-6806
Description
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-9)
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": "64565232-cf19-4134-b9e5-641ef291af47", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["de6e30f8-c8ef-4016-b228-0f188645347b"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-1)", "package_ndc": "68788-6806-1", "marketing_start_date": "20161107"}, {"sample": false, "description": "20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-2)", "package_ndc": "68788-6806-2", "marketing_start_date": "20161107"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-3)", "package_ndc": "68788-6806-3", "marketing_start_date": "20161107"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-6)", "package_ndc": "68788-6806-6", "marketing_start_date": "20161107"}, {"sample": false, "description": "120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-8)", "package_ndc": "68788-6806-8", "marketing_start_date": "20161107"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6806-9)", "package_ndc": "68788-6806-9", "marketing_start_date": "20161107"}], "brand_name": "venlafaxine hydrochloride", "product_id": "68788-6806_64565232-cf19-4134-b9e5-641ef291af47", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-6806", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA090174", "marketing_category": "ANDA", "marketing_start_date": "20161107", "listing_expiration_date": "20261231"}