Package 52427-632-30
Brand: venlafaxine
Generic: venlafaxinePackage Facts
Identity
Package NDC
52427-632-30
Digits Only
5242763230
Product NDC
52427-632
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52427-632-30)
Marketing
Marketing Status
Brand
venlafaxine
Generic
venlafaxine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b0762be-0db0-b997-b76b-b212a496f82c", "openfda": {"upc": ["0352427632303"], "unii": ["18XP3YT5NH"], "rxcui": ["2605950"], "spl_set_id": ["e81a2daf-b8b2-7c05-b532-bc775700b100"], "manufacturer_name": ["Almatica Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (52427-632-30)", "package_ndc": "52427-632-30", "marketing_start_date": "20220801"}], "brand_name": "venlafaxine", "product_id": "52427-632_1b0762be-0db0-b997-b76b-b212a496f82c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "52427-632", "generic_name": "venlafaxine", "labeler_name": "Almatica Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE BESYLATE MONOHYDRATE", "strength": "112.5 mg/1"}], "application_number": "NDA215429", "marketing_category": "NDA", "marketing_start_date": "20220630", "listing_expiration_date": "20261231"}