Package 0378-7002-93

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 0378-7002-93
Digits Only 0378700293
Product NDC 0378-7002
Product ID 0378-7002_b237829d-df98-4a31-b048-91740cf88a63
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7002-93)

Marketing

Marketing Status
Marketed Since 2008-03-24
Brand paroxetine
Generic paroxetine hydrochloride hemihydrate
Sample Package No

Linked Drug Pages (1)

Paroxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b237829d-df98-4a31-b048-91740cf88a63", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["89dd7e24-85fc-4152-89ea-47ec2b48a1ed"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7002-10)", "package_ndc": "0378-7002-10", "marketing_start_date": "20080324"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7002-93)", "package_ndc": "0378-7002-93", "marketing_start_date": "20080324"}], "brand_name": "Paroxetine", "product_id": "0378-7002_b237829d-df98-4a31-b048-91740cf88a63", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0378-7002", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078902", "marketing_category": "ANDA", "marketing_start_date": "20080324", "listing_expiration_date": "20261231"}