sertraline hydrochloride

Generic: sertraline hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sertraline hydrochloride
Generic Name sertraline hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sertraline hydrochloride 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0510
Product ID 71335-0510_8d2426aa-6fc2-48ea-b666-00bfa7084ed5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202825
Listing Expiration 2026-12-31
Marketing Start 2017-02-09

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 713350510
Hyphenated Format 71335-0510

Supplemental Identifiers

RxCUI
312938
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 hydrochloride (source: ndc)
Generic Name sertraline hydrochloride (source: ndc)
Application Number ANDA202825 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0510-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0510-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0510-3)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-0510-4)
  • 28 TABLET, FILM COATED in 1 BOTTLE (71335-0510-5)
  • 15 TABLET, FILM COATED in 1 BOTTLE (71335-0510-6)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-0510-7)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-0510-8)
  • 45 TABLET, FILM COATED in 1 BOTTLE (71335-0510-9)
source: ndc

Packages (9)

Ingredients (1)

sertraline hydrochloride (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8d2426aa-6fc2-48ea-b666-00bfa7084ed5", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["5e91adad-9757-49e4-a3f1-1db0ef396416"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0510-1)", "package_ndc": "71335-0510-1", "marketing_start_date": "20180323"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0510-2)", "package_ndc": "71335-0510-2", "marketing_start_date": "20180321"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0510-3)", "package_ndc": "71335-0510-3", "marketing_start_date": "20180409"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0510-4)", "package_ndc": "71335-0510-4", "marketing_start_date": "20180212"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-0510-5)", "package_ndc": "71335-0510-5", "marketing_start_date": "20240403"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-0510-6)", "package_ndc": "71335-0510-6", "marketing_start_date": "20240403"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0510-7)", "package_ndc": "71335-0510-7", "marketing_start_date": "20240403"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0510-8)", "package_ndc": "71335-0510-8", "marketing_start_date": "20240403"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71335-0510-9)", "package_ndc": "71335-0510-9", "marketing_start_date": "20220831"}], "brand_name": "SERTRALINE HYDROCHLORIDE", "product_id": "71335-0510_8d2426aa-6fc2-48ea-b666-00bfa7084ed5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0510", "generic_name": "SERTRALINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SERTRALINE HYDROCHLORIDE", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA202825", "marketing_category": "ANDA", "marketing_start_date": "20170209", "listing_expiration_date": "20261231"}