Package 50090-5293-0
Brand: desvenlafaxine
Generic: desvenlafaxine succinatePackage Facts
Identity
Package NDC
50090-5293-0
Digits Only
5009052930
Product NDC
50090-5293
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5293-0)
Marketing
Marketing Status
Brand
desvenlafaxine
Generic
desvenlafaxine succinate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "66c3bb56-0642-4ebb-b9ac-7ac6b91843f2", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874559"], "spl_set_id": ["88ac1206-864b-47a3-82ab-be83bc9532f3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5293-0)", "package_ndc": "50090-5293-0", "marketing_start_date": "20201023"}], "brand_name": "Desvenlafaxine", "product_id": "50090-5293_66c3bb56-0642-4ebb-b9ac-7ac6b91843f2", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-5293", "generic_name": "Desvenlafaxine Succinate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204003", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}