Package 70954-319-10
Brand: paroxetine
Generic: paroxetinePackage Facts
Identity
Package NDC
70954-319-10
Digits Only
7095431910
Product NDC
70954-319
Description
250 mL in 1 BOTTLE (70954-319-10)
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": "367bb2bf-beef-4f9a-b045-0c23e9021701", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["312242"], "spl_set_id": ["134e76f0-45cf-47eb-b6e1-cdb3bb522a0a"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BOTTLE (70954-319-10)", "package_ndc": "70954-319-10", "marketing_start_date": "20210903"}], "brand_name": "Paroxetine", "product_id": "70954-319_367bb2bf-beef-4f9a-b045-0c23e9021701", "dosage_form": "SUSPENSION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70954-319", "generic_name": "Paroxetine", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "10 mg/5mL"}], "application_number": "ANDA215003", "marketing_category": "ANDA", "marketing_start_date": "20210903", "listing_expiration_date": "20261231"}