Package 63629-8527-1
Brand: paroxetine hydrochloride
Generic: paroxetine hydrochloridePackage Facts
Identity
Package NDC
63629-8527-1
Digits Only
6362985271
Product NDC
63629-8527
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-8527-1)
Marketing
Marketing Status
Brand
paroxetine hydrochloride
Generic
paroxetine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d72b03fa-f81e-4eab-95aa-00c6c48ebf37", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738805"], "spl_set_id": ["5e47c4fb-6070-4cb4-acaa-c6e90199b55c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-8527-1)", "package_ndc": "63629-8527-1", "marketing_start_date": "20141031"}], "brand_name": "Paroxetine Hydrochloride", "product_id": "63629-8527_d72b03fa-f81e-4eab-95aa-00c6c48ebf37", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63629-8527", "generic_name": "Paroxetine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine Hydrochloride", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "25 mg/1"}], "application_number": "ANDA204744", "marketing_category": "ANDA", "marketing_start_date": "20141031", "listing_expiration_date": "20261231"}