Package 51655-345-26
Brand: sertraline hydrochloride
Generic: sertraline hydrochloridePackage Facts
Identity
Package NDC
51655-345-26
Digits Only
5165534526
Product NDC
51655-345
Description
90 TABLET in 1 BOTTLE, PLASTIC (51655-345-26)
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": "48eb422d-bc39-d06b-e063-6294a90af655", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312940"], "spl_set_id": ["ab30b0a4-6696-19da-e053-2995a90a29aa"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-345-26)", "package_ndc": "51655-345-26", "marketing_start_date": "20200528"}], "brand_name": "Sertraline Hydrochloride", "product_id": "51655-345_48eb422d-bc39-d06b-e063-6294a90af655", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-345", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA077397", "marketing_category": "ANDA", "marketing_start_date": "20200528", "listing_expiration_date": "20271231"}