Package 60760-612-90

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-612-90
Digits Only 6076061290
Product NDC 60760-612
Product ID 60760-612_7f81de84-0ad8-f050-e053-2a91aa0aa762
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-612-90)

Marketing

Marketing Status
Marketed Since 2018-12-26
Brand sertraline hydrochloride
Generic sertraline hydrochloride
Sample Package No

Linked Drug Pages (1)

Sertraline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7f81de84-0ad8-f050-e053-2a91aa0aa762", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["7f81de84-0ad7-f050-e053-2a91aa0aa762"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-612-90)", "package_ndc": "60760-612-90", "marketing_start_date": "20181226"}], "brand_name": "Sertraline Hydrochloride", "product_id": "60760-612_7f81de84-0ad8-f050-e053-2a91aa0aa762", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-612", "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": "50 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20181226", "listing_expiration_date": "20261231"}