sertraline hydrochloride
Generic: sertraline hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
sertraline hydrochloride
Generic Name
sertraline hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sertraline hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-6437
Product ID
68788-6437_a4b57998-b30f-4fde-9675-04c8962cf54d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077206
Listing Expiration
2026-12-31
Marketing Start
2016-07-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687886437
Hyphenated Format
68788-6437
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sertraline hydrochloride (source: ndc)
Generic Name
sertraline hydrochloride (source: ndc)
Application Number
ANDA077206 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (68788-6437-1)
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-6437-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-6437-6)
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-6437-9)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a4b57998-b30f-4fde-9675-04c8962cf54d", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312940"], "spl_set_id": ["b559c20d-70be-41e7-acfb-262ffc3ea878"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-6437-1)", "package_ndc": "68788-6437-1", "marketing_start_date": "20160725"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-6437-3)", "package_ndc": "68788-6437-3", "marketing_start_date": "20160725"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-6437-6)", "package_ndc": "68788-6437-6", "marketing_start_date": "20160725"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-6437-9)", "package_ndc": "68788-6437-9", "marketing_start_date": "20160725"}], "brand_name": "Sertraline Hydrochloride", "product_id": "68788-6437_a4b57998-b30f-4fde-9675-04c8962cf54d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-6437", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20160725", "listing_expiration_date": "20261231"}