Package 70518-3430-2
Brand: paroxetine
Generic: paroxetinePackage Facts
Identity
Package NDC
70518-3430-2
Digits Only
7051834302
Product NDC
70518-3430
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3430-2)
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": "3b8f2e27-57c9-a991-e063-6294a90aba41", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["c002508e-f96c-413b-b232-5d55fceeffe0"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3430-1)", "package_ndc": "70518-3430-1", "marketing_start_date": "20220624"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3430-2)", "package_ndc": "70518-3430-2", "marketing_start_date": "20250801"}], "brand_name": "Paroxetine", "product_id": "70518-3430_3b8f2e27-57c9-a991-e063-6294a90aba41", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-3430", "generic_name": "Paroxetine", "labeler_name": "REMEDYREPACK INC.", "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": "20220602", "listing_expiration_date": "20261231"}