Package 68071-4897-3
Brand: venlafaxine hydrochloride
Generic: venlafaxine hydrochloridePackage Facts
Identity
Package NDC
68071-4897-3
Digits Only
6807148973
Product NDC
68071-4897
Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4897-3)
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": "275d090e-fffd-eb91-e063-6294a90a8ddd", "openfda": {"upc": ["0368071489736"], "unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["8906ed5a-f69c-0eac-e053-2995a90ae600"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4897-3)", "package_ndc": "68071-4897-3", "marketing_start_date": "20190516"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68071-4897_275d090e-fffd-eb91-e063-6294a90a8ddd", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-4897", "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": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}