quetiapine fumarate er

Generic: quetiapine fumarate er

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name quetiapine fumarate er
Generic Name quetiapine fumarate er
Labeler direct_rx
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

quetiapine fumarate 150 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-481
Product ID 72189-481_2c4e167d-290b-0703-e063-6394a90a9132
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090681
Listing Expiration 2026-12-31
Marketing Start 2023-06-01

Pharmacologic Class

Classes
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189481
Hyphenated Format 72189-481

Supplemental Identifiers

RxCUI
895670
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 er (source: ndc)
Generic Name quetiapine fumarate er (source: ndc)
Application Number ANDA090681 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-481-30)
source: ndc

Packages (1)

Ingredients (1)

quetiapine fumarate (150 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4e167d-290b-0703-e063-6394a90a9132", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["895670"], "spl_set_id": ["fd11db2d-364d-9bd6-e053-6394a90ade0b"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-481-30)", "package_ndc": "72189-481-30", "marketing_start_date": "20230601"}], "brand_name": "Quetiapine Fumarate ER", "product_id": "72189-481_2c4e167d-290b-0703-e063-6394a90a9132", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-481", "generic_name": "Quetiapine Fumarate ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate ER", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "150 mg/1"}], "application_number": "ANDA090681", "marketing_category": "ANDA", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}