Package 0574-0279-30
Brand: paroxetine
Generic: paroxetinePackage Facts
Identity
Package NDC
0574-0279-30
Digits Only
0574027930
Product NDC
0574-0279
Description
30 CAPSULE in 1 BOTTLE (0574-0279-30)
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": "2da9c1a5-7b6c-4990-b6a5-1b06e1dd85cd", "openfda": {"unii": ["M711N184JE"], "rxcui": ["1430122"], "spl_set_id": ["1383d713-79b9-45bd-bd06-65707f28bc99"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (0574-0279-30)", "package_ndc": "0574-0279-30", "marketing_start_date": "20171003"}], "brand_name": "Paroxetine", "product_id": "0574-0279_2da9c1a5-7b6c-4990-b6a5-1b06e1dd85cd", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0574-0279", "generic_name": "paroxetine", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE MESYLATE", "strength": "7.5 mg/1"}], "application_number": "NDA204516", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20171003", "listing_expiration_date": "20261231"}