Package 60760-737-90

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-737-90
Digits Only 6076073790
Product NDC 60760-737
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-737-90)

Marketing

Marketing Status
Marketed Since 2018-08-21
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": "f049247b-f016-0ae4-e053-2a95a90a31f5", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["73f4bfe7-80b2-01d8-e053-2991aa0a9cb0"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-737-90)", "package_ndc": "60760-737-90", "marketing_start_date": "20180821"}], "brand_name": "SERTRALINE HYDROCHLORIDE", "product_id": "60760-737_f049247b-f016-0ae4-e053-2a95a90a31f5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-737", "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": "ANDA202825", "marketing_category": "ANDA", "marketing_start_date": "20180821", "listing_expiration_date": "20261231"}