Package 71335-2512-1
Brand: desvenlafaxine
Generic: desvenlafaxinePackage Facts
Identity
Package NDC
71335-2512-1
Digits Only
7133525121
Product NDC
71335-2512
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2512-1)
Marketing
Marketing Status
Brand
desvenlafaxine
Generic
desvenlafaxine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1026998a-300f-406f-9da5-a9e7c346e864", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1874553"], "spl_set_id": ["643bfe62-7885-4db4-9fff-5d8552b53d14"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2512-1)", "package_ndc": "71335-2512-1", "marketing_start_date": "20250604"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2512-2)", "package_ndc": "71335-2512-2", "marketing_start_date": "20250604"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2512-3)", "package_ndc": "71335-2512-3", "marketing_start_date": "20250604"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2512-4)", "package_ndc": "71335-2512-4", "marketing_start_date": "20250604"}], "brand_name": "DESVENLAFAXINE", "product_id": "71335-2512_1026998a-300f-406f-9da5-a9e7c346e864", "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": "71335-2512", "generic_name": "DESVENLAFAXINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESVENLAFAXINE", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA204028", "marketing_category": "ANDA", "marketing_start_date": "20220131", "listing_expiration_date": "20261231"}