Package 60760-738-90

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-738-90
Digits Only 6076073890
Product NDC 60760-738
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-738-90)

Marketing

Marketing Status
Marketed Since 2018-08-09
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": "f06f1ff2-c35e-2929-e053-2a95a90ad1c3", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["730448bf-2d78-44a4-e053-2991aa0ada9e"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-738-90)", "package_ndc": "60760-738-90", "marketing_start_date": "20180809"}], "brand_name": "SERTRALINE HYDROCHLORIDE", "product_id": "60760-738_f06f1ff2-c35e-2929-e053-2a95a90ad1c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-738", "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": "ANDA202825", "marketing_category": "ANDA", "marketing_start_date": "20180809", "listing_expiration_date": "20261231"}