quetiapine fumarate

Generic: quetiapine fumarate

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

Drug Facts

Product Profile

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

quetiapine fumarate 200 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1519
Product ID 71335-1519_33f1decc-af70-5844-e063-6294a90a2a92
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 713351519
Hyphenated Format 71335-1519

Supplemental Identifiers

RxCUI
317174
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 fumarate (source: ndc)
Generic Name quetiapine fumarate (source: ndc)
Application Number ANDA201504 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1519-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-1519-2)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-1519-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1519-4)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1519-5)
source: ndc

Packages (5)

71335-1519-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1519-1) 71335-1519-2 100 TABLET, FILM COATED in 1 BOTTLE (71335-1519-2) 71335-1519-3 120 TABLET, FILM COATED in 1 BOTTLE (71335-1519-3) 71335-1519-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-1519-4) 71335-1519-5 60 TABLET, FILM COATED in 1 BOTTLE (71335-1519-5)

Ingredients (1)

quetiapine fumarate (200 mg/1)

Linked Drug Pages (1)

Quetiapine Fumarate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "33f1decc-af70-5844-e063-6294a90a2a92", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["317174"], "spl_set_id": ["35b2069e-209a-41ac-84e6-377d4f19be87"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1519-1)", "package_ndc": "71335-1519-1", "marketing_start_date": "20200220"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1519-2)", "package_ndc": "71335-1519-2", "marketing_start_date": "20240403"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1519-3)", "package_ndc": "71335-1519-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1519-4)", "package_ndc": "71335-1519-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1519-5)", "package_ndc": "71335-1519-5", "marketing_start_date": "20240403"}], "brand_name": "Quetiapine Fumarate", "product_id": "71335-1519_33f1decc-af70-5844-e063-6294a90a2a92", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-1519", "generic_name": "Quetiapine Fumarate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "200 mg/1"}], "application_number": "ANDA201504", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}