quetiapine

Generic: quetiapine

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

Drug Facts

Product Profile

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

quetiapine fumarate 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1462
Product ID 71335-1462_01261008-5f42-4844-8a65-d4545a67a309
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201504
Listing Expiration 2026-12-31
Marketing Start 2013-03-01

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351462
Hyphenated Format 71335-1462

Supplemental Identifiers

RxCUI
312743
UNII
2S3PL1B6UJ

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 quetiapine (source: ndc)
Generic Name quetiapine (source: ndc)
Application Number ANDA201504 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-1462-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1462-2)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-1462-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1462-4)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1462-5)
  • 15 TABLET, FILM COATED in 1 BOTTLE (71335-1462-6)
source: ndc

Packages (6)

Ingredients (1)

quetiapine fumarate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01261008-5f42-4844-8a65-d4545a67a309", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["312743"], "spl_set_id": ["01261008-5f42-4844-8a65-d4545a67a309"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1462-1)", "package_ndc": "71335-1462-1", "marketing_start_date": "20250627"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1462-2)", "package_ndc": "71335-1462-2", "marketing_start_date": "20200109"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1462-3)", "package_ndc": "71335-1462-3", "marketing_start_date": "20250627"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1462-4)", "package_ndc": "71335-1462-4", "marketing_start_date": "20211110"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1462-5)", "package_ndc": "71335-1462-5", "marketing_start_date": "20200630"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-1462-6)", "package_ndc": "71335-1462-6", "marketing_start_date": "20200214"}], "brand_name": "Quetiapine", "product_id": "71335-1462_01261008-5f42-4844-8a65-d4545a67a309", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-1462", "generic_name": "Quetiapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "100 mg/1"}], "application_number": "ANDA201504", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}