Package 60760-501-90

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 60760-501-90
Digits Only 6076050190
Product NDC 60760-501
Product ID 60760-501_850242ce-1785-a974-e053-2991aa0a4387
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-501-90)

Marketing

Marketing Status
Marketed Since 2019-03-20
Brand paroxetine
Generic paroxetine
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": "850242ce-1785-a974-e053-2991aa0a4387", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738511"], "spl_set_id": ["85020e9f-cff1-8327-e053-2a91aa0abc38"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-501-90)", "package_ndc": "60760-501-90", "marketing_start_date": "20190320"}], "brand_name": "Paroxetine", "product_id": "60760-501_850242ce-1785-a974-e053-2991aa0a4387", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-501", "generic_name": "Paroxetine", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}