Package 71335-0544-3
Brand: paroxetine
Generic: paroxetinePackage Facts
Identity
Package NDC
71335-0544-3
Digits Only
7133505443
Product NDC
71335-0544
Description
90 TABLET, FILM COATED in 1 BOTTLE (71335-0544-3)
Marketing
Marketing Status
Brand
paroxetine
Generic
paroxetine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2586816e-d449-4c27-a592-44ad6a2802da", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["7a702760-9b72-4595-bf47-01aff786c74d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0544-1)", "package_ndc": "71335-0544-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0544-2)", "package_ndc": "71335-0544-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0544-3)", "package_ndc": "71335-0544-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0544-4)", "package_ndc": "71335-0544-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-0544-5)", "package_ndc": "71335-0544-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-0544-6)", "package_ndc": "71335-0544-6", "marketing_start_date": "20220209"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0544-7)", "package_ndc": "71335-0544-7", "marketing_start_date": "20220209"}], "brand_name": "Paroxetine", "product_id": "71335-0544_2586816e-d449-4c27-a592-44ad6a2802da", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0544", "generic_name": "Paroxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20070413", "listing_expiration_date": "20261231"}