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
Routes
ORAL
Active Ingredients

sertraline hydrochloride 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0328
Product ID 71335-0328_0b420eee-e7ab-473f-82ee-254286e4a8aa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077397
Listing Expiration 2026-12-31
Marketing Start 2016-07-21

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 713350328
Hyphenated Format 71335-0328

Supplemental Identifiers

RxCUI
312940
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 ANDA077397 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0328-1)
  • 60 TABLET in 1 BOTTLE (71335-0328-2)
  • 90 TABLET in 1 BOTTLE (71335-0328-3)
  • 180 TABLET in 1 BOTTLE (71335-0328-4)
  • 28 TABLET in 1 BOTTLE (71335-0328-5)
  • 120 TABLET in 1 BOTTLE (71335-0328-6)
source: ndc

Packages (6)

71335-0328-1 30 TABLET in 1 BOTTLE (71335-0328-1) 71335-0328-2 60 TABLET in 1 BOTTLE (71335-0328-2) 71335-0328-3 90 TABLET in 1 BOTTLE (71335-0328-3) 71335-0328-4 180 TABLET in 1 BOTTLE (71335-0328-4) 71335-0328-5 28 TABLET in 1 BOTTLE (71335-0328-5) 71335-0328-6 120 TABLET in 1 BOTTLE (71335-0328-6)

Ingredients (1)

sertraline hydrochloride (25 mg/1)

Linked Drug Pages (1)

Sertraline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0b420eee-e7ab-473f-82ee-254286e4a8aa", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312940"], "spl_set_id": ["22c4b114-5f70-4c64-aa7f-b4169729b847"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0328-1)", "package_ndc": "71335-0328-1", "marketing_start_date": "20180213"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0328-2)", "package_ndc": "71335-0328-2", "marketing_start_date": "20180220"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0328-3)", "package_ndc": "71335-0328-3", "marketing_start_date": "20180226"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0328-4)", "package_ndc": "71335-0328-4", "marketing_start_date": "20211227"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0328-5)", "package_ndc": "71335-0328-5", "marketing_start_date": "20211227"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0328-6)", "package_ndc": "71335-0328-6", "marketing_start_date": "20211227"}], "brand_name": "Sertraline Hydrochloride", "product_id": "71335-0328_0b420eee-e7ab-473f-82ee-254286e4a8aa", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0328", "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": "25 mg/1"}], "application_number": "ANDA077397", "marketing_category": "ANDA", "marketing_start_date": "20160721", "listing_expiration_date": "20261231"}