Package 60760-091-90
Brand: sertraline hydrochloride
Generic: sertraline hydrochloridePackage Facts
Identity
Package NDC
60760-091-90
Digits Only
6076009190
Product NDC
60760-091
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-091-90)
Marketing
Marketing Status
Brand
sertraline hydrochloride
Generic
sertraline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f06d2003-3e24-444a-e053-2995a90a153e", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["8d444aec-cf33-b769-e053-2995a90a54be"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-091-90)", "package_ndc": "60760-091-90", "marketing_start_date": "20190709"}], "brand_name": "Sertraline Hydrochloride", "product_id": "60760-091_f06d2003-3e24-444a-e053-2995a90a153e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-091", "generic_name": "Sertraline Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20190709", "listing_expiration_date": "20261231"}