Package 68071-3727-9
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
68071-3727-9
Digits Only
6807137279
Product NDC
68071-3727
Description
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3727-9)
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": "2787c562-bfc4-cd6d-e063-6294a90aeb00", "openfda": {"upc": ["0368071372793"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["2787aaa2-5210-f7d5-e063-6294a90a7103"], "manufacturer_name": ["NuCare Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3727-9)", "package_ndc": "68071-3727-9", "marketing_start_date": "20241122"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68071-3727_2787c562-bfc4-cd6d-e063-6294a90aeb00", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3727", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}