sertraline

Generic: sertraline

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sertraline
Generic Name sertraline
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sertraline hydrochloride 50 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-818
Product ID 71610-818_3a7784f8-edc2-8cb2-e063-6294a90a8cdc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077397
Listing Expiration 2026-12-31
Marketing Start 2012-08-20

Pharmacologic Class

Classes
cytochrome p450 2d6 inhibitors [moa] serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610818
Hyphenated Format 71610-818

Supplemental Identifiers

RxCUI
312941
UNII
UTI8907Y6X

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 (source: ndc)
Generic Name sertraline (source: ndc)
Application Number ANDA077397 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE (71610-818-15)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71610-818-30)
  • 45 TABLET, FILM COATED in 1 BOTTLE (71610-818-45)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-818-60)
source: ndc

Packages (4)

Ingredients (1)

sertraline hydrochloride (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a7784f8-edc2-8cb2-e063-6294a90a8cdc", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["1548faf9-8625-f871-e063-6394a90a931f"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71610-818-15)", "package_ndc": "71610-818-15", "marketing_start_date": "20240412"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-818-30)", "package_ndc": "71610-818-30", "marketing_start_date": "20250717"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-818-45)", "package_ndc": "71610-818-45", "marketing_start_date": "20240404"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-818-60)", "package_ndc": "71610-818-60", "marketing_start_date": "20240620"}], "brand_name": "SERTRALINE", "product_id": "71610-818_3a7784f8-edc2-8cb2-e063-6294a90a8cdc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-818", "generic_name": "Sertraline", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SERTRALINE", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA077397", "marketing_category": "ANDA", "marketing_start_date": "20120820", "listing_expiration_date": "20261231"}