Package 50090-7692-0

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7692-0
Digits Only 5009076920
Product NDC 50090-7692
Description

90 TABLET in 1 BOTTLE (50090-7692-0)

Marketing

Marketing Status
Marketed Since 2025-10-10
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": "a2b1187a-6b20-4484-a5a3-4b9546dd7380", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["50b54bfa-0b90-44f1-8f73-4f7f552449c4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7692-0)", "package_ndc": "50090-7692-0", "marketing_start_date": "20251010"}], "brand_name": "SERTRALINE HYDROCHLORIDE", "product_id": "50090-7692_a2b1187a-6b20-4484-a5a3-4b9546dd7380", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7692", "generic_name": "sertraline hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SERTRALINE HYDROCHLORIDE", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214790", "marketing_category": "ANDA", "marketing_start_date": "20210503", "listing_expiration_date": "20261231"}